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Anhui Deepblue Medical Technology Co., Ltd.
4th, Floor, D-1 Zone, Pearl Industrial Park, 106 Innovation avenue,
230088
Hefei
China
China
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Our range of products
Product categories
- 03 Diagnostic tests
- 03.02 Immunochemistry testing, immunology testing
- 03.02.02 Diagnostic rapid tests
Diagnostic rapid tests
- COVID-19 (Sars-Cov-2) Antigen Test Kit (Colloidal Gold)
- COVID-19 (Sars-Cov-2) IgG/IgM Antibody Test Kit (Colloidal Gold)
- Influenza A+B & COVID-19 Antigen Combo Test Kit
- Disposable Virus Sampling Tube
- Toxoplasmosis TOXO IGG/IGM Antibody Rapid Diagnostic Blood Test kit
- Dengue NS1 and IgG/IgM Combo Test Kit
- Factory price Professional Use Dengue NS1 Test Kit
- Typhoid IgG/IgM Rapid Test Kit
- Hepatitis B Surface Antigen(HBsAg) Rapid Test
- Syphilis Rapid Test Kit
- H.Pylori Antibody Rapid Test Kit
- Professional Use HCV Rapid Test Kit
- Home Use Factory Price H.Pylori Ag Rapid Test Kit
- Medical Infectious Tuberculosis Bacillus TB Rapid Diagnostic Blood Test kit
- Infectious Disease Rapid Diagnostic Test kit Malaria PF/PV/PAN Test Cassette
- Home Use Fecal Occult Blood (FOB) and TF combo rapid diagnostic feces rapid test kit
- Medical Diagnostic Rapid FOB Test Kit/Feces Occult Blood Test(Colloidal Gold) With CE0123
- Home use One Step HCG Pregnancy Test Strip
- High Sensitivity HCG Pregnancy Urine Test Cassette
- CE Approved HCG Pregnancy Test Midstream
- Best selling cheapest lh ovulation home test strip
- Home Use Self-Testing LH Ovualtion Test Midstream
- Home use One Step LH Ovulation Test Kit
- Individual Packing PROM Insulin-like Growth Factor Binding Protein 1 (IGFBP-1) Rapid Test Kit
Our products
Product category: Diagnostic rapid tests
COVID-19 (Sars-Cov-2) Antigen Test Kit (Colloidal Gold)
This product is used for in vitro qualitative detection of the antigen of SARS-CoV-2 in human Pharyngeal swabs or nasal swabs.
The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection, asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main Manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.
The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection, asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main Manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.
Product category: Diagnostic rapid tests
COVID-19 (Sars-Cov-2) IgG/IgM Antibody Test Kit (Colloidal Gold)
COVID-19（SARS-CoV-2）IgG/IgM Antibody Test is used for qualitative detection of novel coronavirus IgG/IgM antibodies in human serum, plasma and whole blood. After infection with the novel coronavirus, the common signs include respiratory symptoms, fever, cough, wheezing and dyspnea, etc. In more severe cases, the infection can lead to pneumonia, severe acute respiratory syndrome, kidney failure and even death. Coronaviruses can be expelled from the body through respiratory secretions, transmitted by oral fluids, sneezing, contact, and by airborne droplets.
Product category: Diagnostic rapid tests
Influenza A+B & COVID-19 Antigen Combo Test Kit
The Influenza A+B & COVID-19 (SARS-CoV-2) Antigen Test Kit is an in vitro immunochromatographic assay for the qualitative and differential detection of nucleocapsid protein antigen from influenza A, influenza B and SARS-CoV-2 in pharyngeal swab and nasal swab specimens. It is intended to aid in the rapid diagnosis of influenza A, influenza B and SARS-CoV-2 infections.
Product category: Diagnostic rapid tests
Disposable Virus Sampling Tube
[Product Name]: Disposable Virus Sampling Tube
[Specification]: Model: SL-1 (Non inactivated), SL-2 (Inactivated)
[Intended Use]: For the collection, transportation and storage of specimens
[Main components]: It consists of a swab and a tube that containing a viral preservation solution.
[Applicable instrument]: Suitable for use with diagnostic medical instruments for detecting respiratory pathogens.
[Specification]: Model: SL-1 (Non inactivated), SL-2 (Inactivated)
[Intended Use]: For the collection, transportation and storage of specimens
[Main components]: It consists of a swab and a tube that containing a viral preservation solution.
[Applicable instrument]: Suitable for use with diagnostic medical instruments for detecting respiratory pathogens.
Product category: Diagnostic rapid tests
Toxoplasmosis TOXO IGG/IGM Antibody Rapid Diagnostic Blood Test kit
[Product Name]: Toxoplasmosis TOXO IGG/IGM Antibody Rapid Diagnostic Blood Test kit
[Specimen]: Serum/Plasma/ Whole blood
[Read time]:10 minutes
[Storage]: Room Temperature 2--34
[Intend Use] : The One Step TOXO IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Toxoplasma gondii in Whole Blood /Serum / Plasma to aid in the diagnosis of TOXO infection. Toxoplasma gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism. A variety of
serologic tests for antibodies to Toxoplasma gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as The Toxo IgM/IgG Rapid Test (Whole Blood/Serum/Plasma) was introduced into the clinic for the serodiagnosis of Toxoplasma gondii infection. One step TOXO IgG/IgM Test is a simple, visual qualitative test that detects TOXO antibodies in human Whole Blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes.
[Interpretation of Results]:
Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of TOXO specific IgG antibodies. The appearance of T1 test line indicates the presence of TOXO specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both TOXO specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is.
Negative: One colored line appears in the control region(C).No apparent colored line appear in the test line region.
Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
[Specimen]: Serum/Plasma/ Whole blood
[Read time]:10 minutes
[Storage]: Room Temperature 2--34
[Intend Use] : The One Step TOXO IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Toxoplasma gondii in Whole Blood /Serum / Plasma to aid in the diagnosis of TOXO infection. Toxoplasma gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism. A variety of
serologic tests for antibodies to Toxoplasma gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as The Toxo IgM/IgG Rapid Test (Whole Blood/Serum/Plasma) was introduced into the clinic for the serodiagnosis of Toxoplasma gondii infection. One step TOXO IgG/IgM Test is a simple, visual qualitative test that detects TOXO antibodies in human Whole Blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes.
[Interpretation of Results]:
Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of TOXO specific IgG antibodies. The appearance of T1 test line indicates the presence of TOXO specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both TOXO specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is.
Negative: One colored line appears in the control region(C).No apparent colored line appear in the test line region.
Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
Product category: Diagnostic rapid tests
Dengue NS1 and IgG/IgM Combo Test Kit
Dengue combo test NS1 and IgG IgM rapid test
1. Product description--Dengue combo test NS1 and IgG IgM rapid test
Intend to use
The One Step Dengue combo test NS1 and IgG IgM rapid test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen and IGG IGM antibody in Whole Blood /Serum / Plasma to aid in the diagnosis of Dengue viral infection.
2. Test Procedure--Dengue combo test NS1 and IgG IgM rapid test
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
(1). Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
(2). Place the test device on a clean and level surface.
(3). For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.
(4). For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.
(5). Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Packing
As per customer's specified requirements
Standard Export Packing:Carton
Delivery
Small order: By express, TNT/ DHL/ UPS/ Fedex etc.
Large order: By sea or By air
Choose the best suitable way as your need.
1. Product description--Dengue combo test NS1 and IgG IgM rapid test
Intend to use
The One Step Dengue combo test NS1 and IgG IgM rapid test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen and IGG IGM antibody in Whole Blood /Serum / Plasma to aid in the diagnosis of Dengue viral infection.
2. Test Procedure--Dengue combo test NS1 and IgG IgM rapid test
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
(1). Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
(2). Place the test device on a clean and level surface.
(3). For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.
(4). For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.
(5). Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Packing
As per customer's specified requirements
Standard Export Packing:Carton
Delivery
Small order: By express, TNT/ DHL/ UPS/ Fedex etc.
Large order: By sea or By air
Choose the best suitable way as your need.
Product category: Diagnostic rapid tests
Factory price Professional Use Dengue NS1 Test Kit
Intend to use
The One Step Dengue NS1 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen in Whole Blood /Serum / Plasma to aid in the diagnosis of Dengue viral infection.
Test Procedure
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2. Place the test device on a clean and level surface.
3. For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.
4. For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.
5. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
The One Step Dengue NS1 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen in Whole Blood /Serum / Plasma to aid in the diagnosis of Dengue viral infection.
Test Procedure
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2. Place the test device on a clean and level surface.
3. For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.
4. For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.
5. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Product category: Diagnostic rapid tests
Typhoid IgG/IgM Rapid Test Kit
INTENDED USE
The Typhoid IgG/IgM Rapid Test Device（Whole/Serum/Plasma）is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Salmonella typhi in whole blood, serum or plasma specimens to aid in the diagnosis of Salmonella typhi infection.
PRINCIPLE
The Typhoid IgG/IgM Rapid Test Device（Whole/Serum/Plasma）is a qualitative membrane strip based on immunoassay for the detection of Typhoid antibodies (IgG and IgM) in whole blood, serum or plasma specimens. The test device consists of: 1) a burgundy colored conjugate pad containing Typhoid recombinant envelope antigens conjugated with Colloid gold (Typhoid conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgG anti-Typhoid, T2 band is coated with antibody for the detection of IgM anti-Typhoid, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test device, the specimen migrates by capillary action across the device. IgM anti-Typhoid, if present in the specimen, will bind to the Typhoid conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a Typhoid IgM positive test result and suggesting a fresh infection. IgG anti-Typhoid if present in the specimen will bind to the Typhoid conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a Typhoid IgG positive test result and suggesting a recent or repeat infection. Absence of any T bands(T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.
The Typhoid IgG/IgM Rapid Test Device（Whole/Serum/Plasma）is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Salmonella typhi in whole blood, serum or plasma specimens to aid in the diagnosis of Salmonella typhi infection.
PRINCIPLE
The Typhoid IgG/IgM Rapid Test Device（Whole/Serum/Plasma）is a qualitative membrane strip based on immunoassay for the detection of Typhoid antibodies (IgG and IgM) in whole blood, serum or plasma specimens. The test device consists of: 1) a burgundy colored conjugate pad containing Typhoid recombinant envelope antigens conjugated with Colloid gold (Typhoid conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgG anti-Typhoid, T2 band is coated with antibody for the detection of IgM anti-Typhoid, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test device, the specimen migrates by capillary action across the device. IgM anti-Typhoid, if present in the specimen, will bind to the Typhoid conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a Typhoid IgM positive test result and suggesting a fresh infection. IgG anti-Typhoid if present in the specimen will bind to the Typhoid conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a Typhoid IgG positive test result and suggesting a recent or repeat infection. Absence of any T bands(T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.
Product category: Diagnostic rapid tests
Hepatitis B Surface Antigen(HBsAg) Rapid Test
INTENDED USE
HBsAg Rapid Test is a lateral flow immunochromatographic assay for the qualitative determination of Hepatitis B surface antigen (HBsAg) in human whole blood, serum or plasma. It is intended for the screening of blood and blood products to be used for transfusion and an aid for the diagnosis of existing or previous hepatitis B infection.
Principle
The One Step HBsAb Test is a qualitative membrane strip based immunoassay for the detection of Hepatitis B surface Antibody in Whole Blood /Serum / Plasma. In this test procedure, HBsAg is immobilized in the test line region of the device. After a specimen is placed in the specimen well, it reacts with HBsAg coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized HBsAg. If the specimen contains Hepatitis B surface Antibody, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain Hepatitis B surface Antibody, a colored line will not appear in this region indicating a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has
occurred.
HBsAg Rapid Test is a lateral flow immunochromatographic assay for the qualitative determination of Hepatitis B surface antigen (HBsAg) in human whole blood, serum or plasma. It is intended for the screening of blood and blood products to be used for transfusion and an aid for the diagnosis of existing or previous hepatitis B infection.
Principle
The One Step HBsAb Test is a qualitative membrane strip based immunoassay for the detection of Hepatitis B surface Antibody in Whole Blood /Serum / Plasma. In this test procedure, HBsAg is immobilized in the test line region of the device. After a specimen is placed in the specimen well, it reacts with HBsAg coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized HBsAg. If the specimen contains Hepatitis B surface Antibody, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain Hepatitis B surface Antibody, a colored line will not appear in this region indicating a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has
occurred.
Product category: Diagnostic rapid tests
Syphilis Rapid Test Kit
INTENDED USE
The Syphilis Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid visual immunoassay for the qualitative, presumptive detection of IgM and IgG antibodies to Treponema Pallidum (TP) in human whole blood, serum or plasma specimens. This kit is intended for use as an aid in the diagnosis of syphilis.
PRINCIPLE
The Syphilis Rapid Test Device (Whole Blood/Serum/Plasma) detects IgM and IgG antibodies to Treponema Pallidum (TP) through visual interpretation of color development on the internal strip. Specific recombinant TP antigens are immobilized on the test region of the membrane. During testing, the specimen reacts with recombinant TP-specific antigen conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there are sufficient antibodies to Treponema Pallidum (TP) in the specimen, a colored band will form at the test region of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
The Syphilis Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid visual immunoassay for the qualitative, presumptive detection of IgM and IgG antibodies to Treponema Pallidum (TP) in human whole blood, serum or plasma specimens. This kit is intended for use as an aid in the diagnosis of syphilis.
PRINCIPLE
The Syphilis Rapid Test Device (Whole Blood/Serum/Plasma) detects IgM and IgG antibodies to Treponema Pallidum (TP) through visual interpretation of color development on the internal strip. Specific recombinant TP antigens are immobilized on the test region of the membrane. During testing, the specimen reacts with recombinant TP-specific antigen conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there are sufficient antibodies to Treponema Pallidum (TP) in the specimen, a colored band will form at the test region of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
Product category: Diagnostic rapid tests
H.Pylori Antibody Rapid Test Kit
Helicobacter H.Pylori Test Kits Medical Diagnostic Rapid Test Kits
1. Product description--Helicobacter H.Pylori Test Kits Antibody Test Medical Diagnostic Rapid Test Kits
Intend to use
The Helicobacter H.Pylori Test is a qualitative membrane card based immunoassay for the detection of H.pylori antibodies in Whole Blood /Serum / Plasma to aid in the diagnosis of H.pylori.
2. Test Procedure--Helicobacter H.Pylori Test Kits Antibody Test Medical Diagnostic Rapid Test Kits
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
(1). Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
(2). Place the test device on a clean and level surface.
(3). For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.
(4). For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.
Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
1. Product description--Helicobacter H.Pylori Test Kits Antibody Test Medical Diagnostic Rapid Test Kits
Intend to use
The Helicobacter H.Pylori Test is a qualitative membrane card based immunoassay for the detection of H.pylori antibodies in Whole Blood /Serum / Plasma to aid in the diagnosis of H.pylori.
2. Test Procedure--Helicobacter H.Pylori Test Kits Antibody Test Medical Diagnostic Rapid Test Kits
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
(1). Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
(2). Place the test device on a clean and level surface.
(3). For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.
(4). For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.
Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Product category: Diagnostic rapid tests
Professional Use HCV Rapid Test Kit
The One Step HCV Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Hepatitis C Virus (HCV) in Whole Blood /Serum / Plasma to aid in the diagnosis of Hepatitis C Virus infection.
Features
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
Features
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
Product category: Diagnostic rapid tests
Home Use Factory Price H.Pylori Ag Rapid Test Kit
Intend to use
The Helicobacter H.Pylori Test is a qualitative membrane card based immunoassay for the detection of H.pylori antigens in feces
Test Procedure
Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before use.
1. Specimen collection and pre-treatment:
1) Best results will be obtained if the assay is performed within 6 hours after collection.
2) Unscrew and remove the dilution tube applicator. Be careful not to spill or spatter solution from the tube. Collect specimens by inserting the applicator stick into at least 3 different sites of the feces to collect approximately 50 mg of feces (equivalent to 1/4 of a pea).
3) Place the applicator back into the tube and screw the cap tightly. Be careful not to break the tip of the dilution tube.
4) Shake the specimen collection tube vigorously to mix the specimen and the extraction buffer.
2. Testing
1) Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. To obtain a best result, the assay should be performed within one hour.
2) Using a piece of tissue paper, break the tip of the dilution tube. Hold the tube vertically and dispense 2 drops of solution into the specimen well (S) of the test device.Avoid trapping air bubbles in the specimen well (S), and do not drop any solution in observation window.As the test begins to work, you will see color move across the membrane.
3). Wait for the colored band(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.
Note: If the specimen does not migrate (presence of particles), centrifuge the extracted specimens contained in the extraction buffer vial. Collect 80 µL of supernatant, dispense into the specimen well (S) of a new test device and start afresh following the instructions mentioned above.
The Helicobacter H.Pylori Test is a qualitative membrane card based immunoassay for the detection of H.pylori antigens in feces
Test Procedure
Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before use.
1. Specimen collection and pre-treatment:
1) Best results will be obtained if the assay is performed within 6 hours after collection.
2) Unscrew and remove the dilution tube applicator. Be careful not to spill or spatter solution from the tube. Collect specimens by inserting the applicator stick into at least 3 different sites of the feces to collect approximately 50 mg of feces (equivalent to 1/4 of a pea).
3) Place the applicator back into the tube and screw the cap tightly. Be careful not to break the tip of the dilution tube.
4) Shake the specimen collection tube vigorously to mix the specimen and the extraction buffer.
2. Testing
1) Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. To obtain a best result, the assay should be performed within one hour.
2) Using a piece of tissue paper, break the tip of the dilution tube. Hold the tube vertically and dispense 2 drops of solution into the specimen well (S) of the test device.Avoid trapping air bubbles in the specimen well (S), and do not drop any solution in observation window.As the test begins to work, you will see color move across the membrane.
3). Wait for the colored band(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.
Note: If the specimen does not migrate (presence of particles), centrifuge the extracted specimens contained in the extraction buffer vial. Collect 80 µL of supernatant, dispense into the specimen well (S) of a new test device and start afresh following the instructions mentioned above.
Product category: Diagnostic rapid tests
Medical Infectious Tuberculosis Bacillus TB Rapid Diagnostic Blood Test kit
Intended Use
The One Step Tuberculosis Test Cassette is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Tuberculosis (TB) in Whole Blood /Serum / Plasma to aid in the diagnosis of Tuberculosis.
Summary
Tuberculosis (TB) is spread primarily via airborne transmission of aerosolized droplets developed by coughing, sneezing and talking. Areas of poor ventilation pose the greatest risk of exposure to infection. TB is a major cause of morbidity and mortality worldwide, resulting in the greatest number of deaths due to a single infectious agent. The World Health Organization reports that more than 8 million new cases of active tuberculosis are diagnosed annually. Almost 3 million deaths are attributed to TB as well. Timely diagnosis is crucial to TB control, as it provides early initiation of therapy and limits further spread of infection. Several diagnostic methods for detecting TB have been used over the years including skin test, sputum smear, and sputum culture and chest x-ray. But these have severe limitations. Newer tests, such as PCR-DNA amplification or interferon-gamma assay, have been recently introduced. However, the turn-around time for these tests is long, they require laboratory equipment and skilled personnel, and some are neither cost effective nor easy to use. These tests are also expensive and not practical for developing countries. Serological methods constitute an attractive alternative, since TB serodiagnosis is simple, inexpensive, relatively non-invasive, and it does not depend on detection of mycobacteria. The TB Tuberculosis Rapid Test Device (Serum/ Plasma) is a rapid test to qualitatively detect the presence of anti-TB (M. tuberculosis, M. bovis and M. africanum) antibodies (all isotypes: IgG, IgM, IgA, etc.) in Whole Blood/Serum /Plasma. The test utilizes a combination of recombinant antigens to selectively detect elevated levels of anti-TB antibodies in Serum or plasma.
The One Step Tuberculosis Test Cassette is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Tuberculosis (TB) in Whole Blood /Serum / Plasma to aid in the diagnosis of Tuberculosis.
Summary
Tuberculosis (TB) is spread primarily via airborne transmission of aerosolized droplets developed by coughing, sneezing and talking. Areas of poor ventilation pose the greatest risk of exposure to infection. TB is a major cause of morbidity and mortality worldwide, resulting in the greatest number of deaths due to a single infectious agent. The World Health Organization reports that more than 8 million new cases of active tuberculosis are diagnosed annually. Almost 3 million deaths are attributed to TB as well. Timely diagnosis is crucial to TB control, as it provides early initiation of therapy and limits further spread of infection. Several diagnostic methods for detecting TB have been used over the years including skin test, sputum smear, and sputum culture and chest x-ray. But these have severe limitations. Newer tests, such as PCR-DNA amplification or interferon-gamma assay, have been recently introduced. However, the turn-around time for these tests is long, they require laboratory equipment and skilled personnel, and some are neither cost effective nor easy to use. These tests are also expensive and not practical for developing countries. Serological methods constitute an attractive alternative, since TB serodiagnosis is simple, inexpensive, relatively non-invasive, and it does not depend on detection of mycobacteria. The TB Tuberculosis Rapid Test Device (Serum/ Plasma) is a rapid test to qualitatively detect the presence of anti-TB (M. tuberculosis, M. bovis and M. africanum) antibodies (all isotypes: IgG, IgM, IgA, etc.) in Whole Blood/Serum /Plasma. The test utilizes a combination of recombinant antigens to selectively detect elevated levels of anti-TB antibodies in Serum or plasma.
Product category: Diagnostic rapid tests
Infectious Disease Rapid Diagnostic Test kit Malaria PF/PV/PAN Test Cassette
INTENDED USE
The Malaria P.f./P.v. Rapid Test Device (Whole blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of two kinds of circulating Plasmodium falciparum (P.f.) and Plasmodium vivax (P.v.) in whole blood, serum or plasma.
PRINCIPLE
The Malaria P.f./P.v. Rapid Test Device (Whole blood/Serum/Plasma) is a qualitative, membrane based immunoassay for the detection of P.f and P.v antigens in whole blood, serum or plasma. The membrane is pre-coated with anti-HRP-II antibodies and anti-pLDH antibodies. During testing, the specimen reacts with the dye conjugate, which has been pre-coated on the test strip. The mixture then migrates upward on the membrane by capillary action, reacts with anti-Histidine-Rich Protein II (HRP-II) antibodies on the membrane on P.f Test Line region and with anti-pLDH antibodies on the membrane on P.v. Line region. If the specimen contains HRP-II or Plasmodium-specific P.vivaLDH or both, a colored line will appear in P.f line region or P.v. line region or two colored lines will appear in P.f line region and P.v. line region. The absence of the colored lines in P.f line region or P.v. line region indicates that the specimen does not contain HRP-II and/or Plasmodium-specific P.vivaLDH. To serve as a procedure control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.
The Malaria P.f./P.v. Rapid Test Device (Whole blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of two kinds of circulating Plasmodium falciparum (P.f.) and Plasmodium vivax (P.v.) in whole blood, serum or plasma.
PRINCIPLE
The Malaria P.f./P.v. Rapid Test Device (Whole blood/Serum/Plasma) is a qualitative, membrane based immunoassay for the detection of P.f and P.v antigens in whole blood, serum or plasma. The membrane is pre-coated with anti-HRP-II antibodies and anti-pLDH antibodies. During testing, the specimen reacts with the dye conjugate, which has been pre-coated on the test strip. The mixture then migrates upward on the membrane by capillary action, reacts with anti-Histidine-Rich Protein II (HRP-II) antibodies on the membrane on P.f Test Line region and with anti-pLDH antibodies on the membrane on P.v. Line region. If the specimen contains HRP-II or Plasmodium-specific P.vivaLDH or both, a colored line will appear in P.f line region or P.v. line region or two colored lines will appear in P.f line region and P.v. line region. The absence of the colored lines in P.f line region or P.v. line region indicates that the specimen does not contain HRP-II and/or Plasmodium-specific P.vivaLDH. To serve as a procedure control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.
Product category: Diagnostic rapid tests
Home Use Fecal Occult Blood (FOB) and TF combo rapid diagnostic feces rapid test kit
Intended Use
The Fecal Occult Blood & Transferrin Test (Colloidal Gold) is a qualitative test that detects human hemoglobin and transferrin in human fecal specimens. The test is a visual one step, in-vitro assay. It is intended for professional use to help diagnose gastrointestinal bleeding.
Principle
The Fecal Occult Blood & Transferrin Test (Colloidal Gold) is a lateral flow chromatographic immunoassay for the qualitative detection of hemoglobin and /or Transferrin hemoglobinin human feces.The membrane is pre-coated with anti-transferrin antibody and anti- hemoglobin antibody on the test line region of the strip. During testing, the specimen with hemoglobin and/or transferrin reacts with the particle coated with anti-transferrin antibody or anti-hemoglobin antibody ,the mixture migrates upward on the membrane chromatographically by capillary action to react with anti-transferrin antibody and /or anti- hemoglobin antibody on the membrane and generate a colored line. The presence of red band in the testing area(H) and (T),indicates a positive result for hemoglobin and/or transferrin. While absence of red band in testing area(H) and /or (T), indicates hemoglobin and/or transferrin is negative result.To serve as a procedural control, a colored line will always appear in the control line region indicating that the proper volume of specimen has been added and membrane wicking has occurred.
The Fecal Occult Blood & Transferrin Test (Colloidal Gold) is a qualitative test that detects human hemoglobin and transferrin in human fecal specimens. The test is a visual one step, in-vitro assay. It is intended for professional use to help diagnose gastrointestinal bleeding.
Principle
The Fecal Occult Blood & Transferrin Test (Colloidal Gold) is a lateral flow chromatographic immunoassay for the qualitative detection of hemoglobin and /or Transferrin hemoglobinin human feces.The membrane is pre-coated with anti-transferrin antibody and anti- hemoglobin antibody on the test line region of the strip. During testing, the specimen with hemoglobin and/or transferrin reacts with the particle coated with anti-transferrin antibody or anti-hemoglobin antibody ,the mixture migrates upward on the membrane chromatographically by capillary action to react with anti-transferrin antibody and /or anti- hemoglobin antibody on the membrane and generate a colored line. The presence of red band in the testing area(H) and (T),indicates a positive result for hemoglobin and/or transferrin. While absence of red band in testing area(H) and /or (T), indicates hemoglobin and/or transferrin is negative result.To serve as a procedural control, a colored line will always appear in the control line region indicating that the proper volume of specimen has been added and membrane wicking has occurred.
Product category: Diagnostic rapid tests
Medical Diagnostic Rapid FOB Test Kit/Feces Occult Blood Test(Colloidal Gold) With CE0123
Intended Use
Fecal Occult Blood (FOB) Test (Colloidal Gold) is used for qualitative detection of hemoglobin in human feces at home for self-testing, or at all levels of medical institutions for testing, so as to provide auxiliary diagnosis for digestive tract haemorrhagic disease.
Principle
This assay is a one-step lateral flow chromatographic immunoassay. The test strip consists of: 1) a burgundy colored conjugate pad containing mouse anti-hHb antibodies conjugated with colloidal gold and 2) a nitrocellulose membrane strip containing a Test line (T-line) and a Control line (C-line). The T-line is coated with anti-hHb antibodies, and the C-line is coated with goat anti-mouse IgG antibodies.
When an adequate volume of test specimen is dispensed into the sample well of the device, the test specimen migrates by capillary action across the test strip. If the concentration of hHb in the specimen is at or above 50 ng/ml, the T-line appears as a visible burgundy line. If the concentration of hHb in the specimen is below the detectable level, no T-line develops. The C-line is coated with goat anti-mouse antibody, which binds to the conjugated monoclonal antibody, regardless of the presence of hHb in the sample.
Fecal Occult Blood (FOB) Test (Colloidal Gold) is used for qualitative detection of hemoglobin in human feces at home for self-testing, or at all levels of medical institutions for testing, so as to provide auxiliary diagnosis for digestive tract haemorrhagic disease.
Principle
This assay is a one-step lateral flow chromatographic immunoassay. The test strip consists of: 1) a burgundy colored conjugate pad containing mouse anti-hHb antibodies conjugated with colloidal gold and 2) a nitrocellulose membrane strip containing a Test line (T-line) and a Control line (C-line). The T-line is coated with anti-hHb antibodies, and the C-line is coated with goat anti-mouse IgG antibodies.
When an adequate volume of test specimen is dispensed into the sample well of the device, the test specimen migrates by capillary action across the test strip. If the concentration of hHb in the specimen is at or above 50 ng/ml, the T-line appears as a visible burgundy line. If the concentration of hHb in the specimen is below the detectable level, no T-line develops. The C-line is coated with goat anti-mouse antibody, which binds to the conjugated monoclonal antibody, regardless of the presence of hHb in the sample.
Product category: Diagnostic rapid tests
Home use One Step HCG Pregnancy Test Strip
Intended Use
HCG Pregnancy Test (Colloidal Gold) is used for all levels of medical institutions for early diagnosis of patients with early pregnancy and patients at home for self-testing.
Principle
The HCG Pregnancy Test Strip utilizes a combination of antibodies including a monoclonal HCG antibody to selectively detect elevated levels of HCG. The assay is conducted by immersing the test in a urine specimen and observing the formation of red-colored lines. The specimen migrates via capillary action along the membrane to react with the colored conjugate. Positive specimens react with the specific antibody-HCG-colored conjugate and form a red colored line at the test line region of the membrane. The absence of this red colored line suggests a negative result. To serve as a procedural control, a red colored line will always appear in the control line region if the test has been performed properly.
Key Features:
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
5. High accuracy verified by clinical tests
HCG Pregnancy Test (Colloidal Gold) is used for all levels of medical institutions for early diagnosis of patients with early pregnancy and patients at home for self-testing.
Principle
The HCG Pregnancy Test Strip utilizes a combination of antibodies including a monoclonal HCG antibody to selectively detect elevated levels of HCG. The assay is conducted by immersing the test in a urine specimen and observing the formation of red-colored lines. The specimen migrates via capillary action along the membrane to react with the colored conjugate. Positive specimens react with the specific antibody-HCG-colored conjugate and form a red colored line at the test line region of the membrane. The absence of this red colored line suggests a negative result. To serve as a procedural control, a red colored line will always appear in the control line region if the test has been performed properly.
Key Features:
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
5. High accuracy verified by clinical tests
Product category: Diagnostic rapid tests
High Sensitivity HCG Pregnancy Urine Test Cassette
Intended use
HCG Pregnancy Test (Colloidal Gold) is used for all levels of medical institutions for early diagnosis of patients with early pregnancy and patients at home for self-testing.
Principle
The HCG Pregnancy Test Cassette utilizes a combination of antibodies including a monoclonal HCG antibody to selectively detect elevated levels of HCG. The assay is conducted by filling the urine specimen to sample well and observing the formation of red-colored lines. The specimen migrates via capillary action along the membrane to react with the colored conjugate. Positive specimens react with the specific antibody-HCG-colored conjugate and form a red colored line at the test line region of the membrane. The absence of this red colored line suggests a negative result. To serve as a procedural control, a red colored line will always appear in the control line region if the test has been performed properly.
Features
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
5. High accuracy verified by clinical tests
HCG Pregnancy Test (Colloidal Gold) is used for all levels of medical institutions for early diagnosis of patients with early pregnancy and patients at home for self-testing.
Principle
The HCG Pregnancy Test Cassette utilizes a combination of antibodies including a monoclonal HCG antibody to selectively detect elevated levels of HCG. The assay is conducted by filling the urine specimen to sample well and observing the formation of red-colored lines. The specimen migrates via capillary action along the membrane to react with the colored conjugate. Positive specimens react with the specific antibody-HCG-colored conjugate and form a red colored line at the test line region of the membrane. The absence of this red colored line suggests a negative result. To serve as a procedural control, a red colored line will always appear in the control line region if the test has been performed properly.
Features
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
5. High accuracy verified by clinical tests
Product category: Diagnostic rapid tests
CE Approved HCG Pregnancy Test Midstream
Intended use
HCG Pregnancy Test (Colloidal Gold) is used for all levels of medical institutions for early diagnosis of patients with early pregnancy and patients at home for self-testing.
Principle
The HCG Pregnancy Test Midstream utilizes a combination of antibodies including a monoclonal HCG antibody to selectively detect elevated levels of HCG. The assay is conducted by filling the urine specimen to sample well and observing the formation of red-colored lines. The specimen migrates via capillary action along the membrane to react with the colored conjugate. Positive specimens react with the specific antibody-HCG-colored conjugate and form a red colored line at the test line region of the membrane. The absence of this red colored line suggests a negative result. To serve as a procedural control, a red colored line will always appear in the control line region if the test has been performed properly.
Features
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
5. High accuracy verified by clinical tests
Sensitivity
10 miu/ml 25 miu/ml
HCG Pregnancy Test (Colloidal Gold) is used for all levels of medical institutions for early diagnosis of patients with early pregnancy and patients at home for self-testing.
Principle
The HCG Pregnancy Test Midstream utilizes a combination of antibodies including a monoclonal HCG antibody to selectively detect elevated levels of HCG. The assay is conducted by filling the urine specimen to sample well and observing the formation of red-colored lines. The specimen migrates via capillary action along the membrane to react with the colored conjugate. Positive specimens react with the specific antibody-HCG-colored conjugate and form a red colored line at the test line region of the membrane. The absence of this red colored line suggests a negative result. To serve as a procedural control, a red colored line will always appear in the control line region if the test has been performed properly.
Features
1. High specificity and sensitivity
2. Simple operation and one-step detection
3. Rapid testing and the results will be in 3-5 minutes
4. Clear background and easy to read
5. High accuracy verified by clinical tests
Sensitivity
10 miu/ml 25 miu/ml
Product category: Diagnostic rapid tests
Best selling cheapest lh ovulation home test strip
Intended Use
LH Ovulation Test (Colloidal Gold) is a qualitative test used to predict when there is a LH surge, and in turn, when you are likely to ovulate.
LH Ovulation Test (Colloidal Gold) is used to detect the concentration of LH in urine in all levels of medical institutions and at home for self-testing.
Principle
LH Ovulation Test Strip is a kind of hormone, the content of which changes periodically with the female menstrual cycle. Its effect is to stimulate the release of mature eggs within the ovaries. When its peak appears, LH abounds in the blood and urine of female. Therefore, the detection of LH in urine is a reliable criterion for the prediction of ovulation. The ovulation test strip adopts the principle of chromatographic double antibody sandwich method to detect the level of LH, and is adequate for family self-test. It is helpful to improve the success ratio of pregnancy or can be used as a reference to contraception and an auxiliary diagnosis for clinical prediction of ovulation cycle.
Performance Characteristics
Detection limit: The detection limit of LH Ovulation Test Strip is 25 mIU/ml.
Specificity: To test by 0 mIU/ml LH mixed sample solution with, 50 mIU/ml FSH, and 50μIU/mL TSH, the results shall be all negative.
Repeatability: The results should be consistent and the coloration degree should be consistent when detecting the 50mIU/ml, 25mIU/ml, 12.5mIU/ml of LH standards by 10 kits of the same batch.
Hook effect: When the concentration of LH exceeds 2000mIU/ml, the coloration of the test will decrease and the detection result may be false negative, and should be diluted and test again.
HAMA (human anti-mouse antibody) interference: 20ng/mL HAMA has no effect on the detection results of hCG reagent.
Analytical sensitivity: Hematuresis (Hb concentration of 1.8g/L), bilirubinuria (85μmol/L) and proteinuria (5.65mmol/L) has no effect on the detection results.
Diagnostic specificity and sensitivity: A clinical evaluation was conducted on 200 specimens (including 94 positive specimens and 106 negative specimens) comparing the results obtained using the LH Ovulation Test (Colloidal Gold) and other commercially available LH tests.
LH Ovulation Test (Colloidal Gold) is a qualitative test used to predict when there is a LH surge, and in turn, when you are likely to ovulate.
LH Ovulation Test (Colloidal Gold) is used to detect the concentration of LH in urine in all levels of medical institutions and at home for self-testing.
Principle
LH Ovulation Test Strip is a kind of hormone, the content of which changes periodically with the female menstrual cycle. Its effect is to stimulate the release of mature eggs within the ovaries. When its peak appears, LH abounds in the blood and urine of female. Therefore, the detection of LH in urine is a reliable criterion for the prediction of ovulation. The ovulation test strip adopts the principle of chromatographic double antibody sandwich method to detect the level of LH, and is adequate for family self-test. It is helpful to improve the success ratio of pregnancy or can be used as a reference to contraception and an auxiliary diagnosis for clinical prediction of ovulation cycle.
Performance Characteristics
Detection limit: The detection limit of LH Ovulation Test Strip is 25 mIU/ml.
Specificity: To test by 0 mIU/ml LH mixed sample solution with, 50 mIU/ml FSH, and 50μIU/mL TSH, the results shall be all negative.
Repeatability: The results should be consistent and the coloration degree should be consistent when detecting the 50mIU/ml, 25mIU/ml, 12.5mIU/ml of LH standards by 10 kits of the same batch.
Hook effect: When the concentration of LH exceeds 2000mIU/ml, the coloration of the test will decrease and the detection result may be false negative, and should be diluted and test again.
HAMA (human anti-mouse antibody) interference: 20ng/mL HAMA has no effect on the detection results of hCG reagent.
Analytical sensitivity: Hematuresis (Hb concentration of 1.8g/L), bilirubinuria (85μmol/L) and proteinuria (5.65mmol/L) has no effect on the detection results.
Diagnostic specificity and sensitivity: A clinical evaluation was conducted on 200 specimens (including 94 positive specimens and 106 negative specimens) comparing the results obtained using the LH Ovulation Test (Colloidal Gold) and other commercially available LH tests.
Product category: Diagnostic rapid tests
Home Use Self-Testing LH Ovualtion Test Midstream
Intended Use
LH Ovulation Test (Colloidal Gold) is a qualitative test used to predict when there is a LH surge, and in turn, when you are likely to ovulate.
LH Ovulation Test (Colloidal Gold) is used to detect the concentration of LH in urine in all levels of medical institutions and at home for self-testing.
Principle
LH Ovulation Test Midstream is a kind of hormone, the content of which changes periodically with the female menstrual cycle. Its effect is to stimulate the release of mature eggs within the ovaries. When its peak appears, LH abounds in the blood and urine of female. Therefore, the detection of LH in urine is a reliable criterion for the prediction of ovulation. The ovulation test strip adopts the principle of chromatographic double antibody sandwich method to detect the level of LH, and is adequate for family self-test. It is helpful to improve the success ratio of pregnancy or can be used as a reference to contraception and an auxiliary diagnosis for clinical prediction of ovulation cycle.
Performance Characteristics
Detection limit: The detection limit of LH Ovulation Test Midstream is 25 mIU/ml.
Specificity: To test by 0 mIU/ml LH mixed sample solution with, 50 mIU/ml FSH, and 50μIU/mL TSH, the results shall be all negative.
Repeatability: The results should be consistent and the coloration degree should be consistent when detecting the 50mIU/ml, 25mIU/ml, 12.5mIU/ml of LH standards by 10 kits of the same batch.
Hook effect: When the concentration of LH exceeds 2000mIU/ml, the coloration of the test will decrease and the detection result may be false negative, and should be diluted and test again.
HAMA (human anti-mouse antibody) interference: 20ng/mL HAMA has no effect on the detection results of hCG reagent.
Analytical sensitivity: Hematuresis (Hb concentration of 1.8g/L), bilirubinuria (85μmol/L) and proteinuria (5.65mmol/L) has no effect on the detection results.
LH Ovulation Test (Colloidal Gold) is a qualitative test used to predict when there is a LH surge, and in turn, when you are likely to ovulate.
LH Ovulation Test (Colloidal Gold) is used to detect the concentration of LH in urine in all levels of medical institutions and at home for self-testing.
Principle
LH Ovulation Test Midstream is a kind of hormone, the content of which changes periodically with the female menstrual cycle. Its effect is to stimulate the release of mature eggs within the ovaries. When its peak appears, LH abounds in the blood and urine of female. Therefore, the detection of LH in urine is a reliable criterion for the prediction of ovulation. The ovulation test strip adopts the principle of chromatographic double antibody sandwich method to detect the level of LH, and is adequate for family self-test. It is helpful to improve the success ratio of pregnancy or can be used as a reference to contraception and an auxiliary diagnosis for clinical prediction of ovulation cycle.
Performance Characteristics
Detection limit: The detection limit of LH Ovulation Test Midstream is 25 mIU/ml.
Specificity: To test by 0 mIU/ml LH mixed sample solution with, 50 mIU/ml FSH, and 50μIU/mL TSH, the results shall be all negative.
Repeatability: The results should be consistent and the coloration degree should be consistent when detecting the 50mIU/ml, 25mIU/ml, 12.5mIU/ml of LH standards by 10 kits of the same batch.
Hook effect: When the concentration of LH exceeds 2000mIU/ml, the coloration of the test will decrease and the detection result may be false negative, and should be diluted and test again.
HAMA (human anti-mouse antibody) interference: 20ng/mL HAMA has no effect on the detection results of hCG reagent.
Analytical sensitivity: Hematuresis (Hb concentration of 1.8g/L), bilirubinuria (85μmol/L) and proteinuria (5.65mmol/L) has no effect on the detection results.
Product category: Diagnostic rapid tests
Home use One Step LH Ovulation Test Kit
Intended Use
LH Ovulation Test (Colloidal Gold) is a qualitative test used to predict when there is a LH surge, and in turn, when you are likely to ovulate.
LH Ovulation Test (Colloidal Gold) is used to detect the concentration of LH in urine in all levels of medical institutions and at home for self-testing.
Principle
LH Ovulation Test Midstream is a kind of hormone, the content of which changes periodically with the female menstrual cycle. Its effect is to stimulate the release of mature eggs within the ovaries. When its peak appears, LH abounds in the blood and urine of female. Therefore, the detection of LH in urine is a reliable criterion for the prediction of ovulation. The ovulation test strip adopts the principle of chromatographic double antibody sandwich method to detect the level of LH, and is adequate for family self-test. It is helpful to improve the success ratio of pregnancy or can be used as a reference to contraception and an auxiliary diagnosis for clinical prediction of ovulation cycle.
Performance Characteristics
Detection limit: The detection limit of LH Ovulation Test Midstream is 25 mIU/ml.
Specificity: To test by 0 mIU/ml LH mixed sample solution with, 50 mIU/ml FSH, and 50μIU/mL TSH, the results shall be all negative.
Repeatability: The results should be consistent and the coloration degree should be consistent when detecting the 50mIU/ml, 25mIU/ml, 12.5mIU/ml of LH standards by 10 kits of the same batch.
Hook effect: When the concentration of LH exceeds 2000mIU/ml, the coloration of the test will decrease and the detection result may be false negative, and should be diluted and test again.
HAMA (human anti-mouse antibody) interference: 20ng/mL HAMA has no effect on the detection results of hCG reagent.
Analytical sensitivity: Hematuresis (Hb concentration of 1.8g/L), bilirubinuria (85μmol/L) and proteinuria (5.65mmol/L) has no effect on the detection results.
LH Ovulation Test (Colloidal Gold) is a qualitative test used to predict when there is a LH surge, and in turn, when you are likely to ovulate.
LH Ovulation Test (Colloidal Gold) is used to detect the concentration of LH in urine in all levels of medical institutions and at home for self-testing.
Principle
LH Ovulation Test Midstream is a kind of hormone, the content of which changes periodically with the female menstrual cycle. Its effect is to stimulate the release of mature eggs within the ovaries. When its peak appears, LH abounds in the blood and urine of female. Therefore, the detection of LH in urine is a reliable criterion for the prediction of ovulation. The ovulation test strip adopts the principle of chromatographic double antibody sandwich method to detect the level of LH, and is adequate for family self-test. It is helpful to improve the success ratio of pregnancy or can be used as a reference to contraception and an auxiliary diagnosis for clinical prediction of ovulation cycle.
Performance Characteristics
Detection limit: The detection limit of LH Ovulation Test Midstream is 25 mIU/ml.
Specificity: To test by 0 mIU/ml LH mixed sample solution with, 50 mIU/ml FSH, and 50μIU/mL TSH, the results shall be all negative.
Repeatability: The results should be consistent and the coloration degree should be consistent when detecting the 50mIU/ml, 25mIU/ml, 12.5mIU/ml of LH standards by 10 kits of the same batch.
Hook effect: When the concentration of LH exceeds 2000mIU/ml, the coloration of the test will decrease and the detection result may be false negative, and should be diluted and test again.
HAMA (human anti-mouse antibody) interference: 20ng/mL HAMA has no effect on the detection results of hCG reagent.
Analytical sensitivity: Hematuresis (Hb concentration of 1.8g/L), bilirubinuria (85μmol/L) and proteinuria (5.65mmol/L) has no effect on the detection results.
Product category: Diagnostic rapid tests
Individual Packing PROM Insulin-like Growth Factor Binding Protein 1 (IGFBP-1) Rapid Test Kit
Intended use
The PROM Rapid Test is a rapid qualitative immunochromatographic test for the detection of IGFBP-1 in vaginal secretions. The test is intended for use by health care professionals as an aid in the diagnosis of premature rupture of amniotic membranes (prom) in pregnant women where prom is suspected.
Interpretation of Results
Negative: Only one colored band appears on the control region. No apparent band on the test region.
Positive: In addition to a pink colored control band, a distinct pink colored band will also appear in the test region.
Invalid: A total absence of color in both regions is an indication of procedure error and/or that test reagent deterioration has occurred.
Features
1). Specific to human Insulin-like growth factor binding protein-1 (IGFBP-1)of Amniotic Fluid
2). No interference to blood, urine, or cervical mucus
3). Easy to interpret, no need for instrumentation
4). Simple operation and could be used at home
The PROM Rapid Test is a rapid qualitative immunochromatographic test for the detection of IGFBP-1 in vaginal secretions. The test is intended for use by health care professionals as an aid in the diagnosis of premature rupture of amniotic membranes (prom) in pregnant women where prom is suspected.
Interpretation of Results
Negative: Only one colored band appears on the control region. No apparent band on the test region.
Positive: In addition to a pink colored control band, a distinct pink colored band will also appear in the test region.
Invalid: A total absence of color in both regions is an indication of procedure error and/or that test reagent deterioration has occurred.
Features
1). Specific to human Insulin-like growth factor binding protein-1 (IGFBP-1)of Amniotic Fluid
2). No interference to blood, urine, or cervical mucus
3). Easy to interpret, no need for instrumentation
4). Simple operation and could be used at home
Company news
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Nov 15, 2020
COVID-19 (Sars-Cov-2) Rapid Test Kit was register in over 20 Countries!
Anhui DeepBlue Medical Technology Co., Ltd. is the first batch white list enterprise that approved by the Ministry of Commerce to export the COVID-19 Rapid test kit.
Since March 2020, the International Trade Department of DeepBlue has been working overtime to actively assist foreign customers in product registration, so as to ensure the fastest speed to help screen infected patients and reduce the spread of the virus. For now, the COVID-19 (Sars-CoV-2) IgG/IgM Antibodt test kit and COVID-19 (Sars-CoV-2) Antigen Test kit that manufactured by Deepblue Medical has been successively registered in over 20 countries, including Germany, Italy, Portugal, Mexico, Brazil and so on.
Since March 2020, the International Trade Department of DeepBlue has been working overtime to actively assist foreign customers in product registration, so as to ensure the fastest speed to help screen infected patients and reduce the spread of the virus. For now, the COVID-19 (Sars-CoV-2) IgG/IgM Antibodt test kit and COVID-19 (Sars-CoV-2) Antigen Test kit that manufactured by Deepblue Medical has been successively registered in over 20 countries, including Germany, Italy, Portugal, Mexico, Brazil and so on.
About us
Company details
Anhui DeepBlue Medical Technology Co., Ltd. was established in February 4, 2010 and located in Hefei High-tech Zone, Anhui, China. DeepBlue Medical is a Chinese high-tech enterprise specialized in R&D, manufacturing, marketing and after-sales service of diagnostic reagents and biological raw materials.
DeepBlue Medical have advanced rapid diagnostic reagent production lines and the latest clinical testing technologies. The products have many advantages such as simple operation, accurate and reliable, timely and convenient and so on. its technical performance has been to the domestic advanced level. Deepblue Medical has already passed the CE and ISO13485 quality management system.
Our main products are COVID-19 (Sars-Cov-2) Antigen Test Kit, COVID-19 (Sars-Cov-2) IgG/IgM Antibody Test Kit , HCG Pregnancy Test, LH Ovulation Test , Fecal Occult Blood Test series, IGFBP-1 PROM Test Kits, Other Infectious Disease Test Series (Flu A/B, Malaria, Dengue, HIV, H pylori and so on). We are looking forward to establish a long-term cooperation with you in the near future!
DeepBlue Medical have advanced rapid diagnostic reagent production lines and the latest clinical testing technologies. The products have many advantages such as simple operation, accurate and reliable, timely and convenient and so on. its technical performance has been to the domestic advanced level. Deepblue Medical has already passed the CE and ISO13485 quality management system.
Our main products are COVID-19 (Sars-Cov-2) Antigen Test Kit, COVID-19 (Sars-Cov-2) IgG/IgM Antibody Test Kit , HCG Pregnancy Test, LH Ovulation Test , Fecal Occult Blood Test series, IGFBP-1 PROM Test Kits, Other Infectious Disease Test Series (Flu A/B, Malaria, Dengue, HIV, H pylori and so on). We are looking forward to establish a long-term cooperation with you in the near future!
Company data
Sales volume10-49 Mio US $
Export content> 75%
Number of employees100-499
Foundation2010
Area of businessDiagnostics