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Buy AccuTest Malaria Pf(HRP II)/Pv Rapid Card Test (50 Tests) Online from Accurex. This Malaria test is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. This Malaria parasite test kit has test strips coated with Monoclonal Anti-p LDH antibodies (test line Pv) specific to the lactate dehydrogenase of P. vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P. falciparum. AccuTest Malaria Pf(HRP II)/Pv is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. PRINCIPLE: AccuTest Malaria Pf (HRP II)/Pv test utilizes the principle of immuno-chromatography. It has the test strip coated with Monoclonal Anti-pLDH antibodies (test line Pv) specific to the lactate dehydrogenase of P.vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P.falciparum. As the test sample flows through the membrane assembly of the device after addition of the buffer solution, the colored colloidal gold, anti-pLDH antibody and the anti-HRP-II antibody conjugate complexes with the lysed blood sample. The Malaria antigens get immobilized on the respective test lines on the nitrocellulose membrane which leads to the formation of red/purple colored band/s. The un-reacted conjugate and unbound complex if any moves further on the membrane and are subsequently immobilized at the control “C” region forming a red/purple band. This control band serves to validate the test performance and should always appear. This test is intended for professional use and must be used by trained personnel. Related products Safety Information PRECAUTIONS: 1. For in-vitro diagnostic use only. 2. The device is sensitive to humidity as well as to heat. So, it’s very important to take out the device from the sealed pouch just before use. 3. Do not use the kit after the expiration date. 4. Dispose all the samples and kits properly after test, in accordance with GLP. 5. Do not pipette reagent or blood by mouth. Direction for Use Procedure: 1. Disinfect with alcohol swab 2. Punture by lancet 3. Collect blood upto marking on sample dropper Other Info STORAGE AND EXPIRATION: 1. AccuTest Malaria Pf(HRP II)/Pv test kit should be stored between 4 – 30ºC. 2. Expiration date of this kit is 18 months after its manufacture date.

Buy AccuTest HIV – 1/2 Ab Rapid Card Test (50 Tests) Online from Accurex. This Rapid HIV test is a visual, solid phase immunochromatographic assay for qualitative in-vitro diagnostic detection of antibodies against HIV-1 and HIV-2 in human serum/plasma. This HIV test may be used as an aid in diagnosis of HIV infection. In the HIV blood test – A reactive result should be confirmed by supplemental testing as part of a validated HIV testing algorithm. INTENDED USE: AccuTest HIV – 1/2 Ab test is a visual, solid phase immunochromatographic assay for qualitative in-vitro diagnostic detection of antibodies against HIV-1 and HIV-2 in human serum/plasma. The product may be used as an aid in diagnosis of HIV infection. A reactive result should be confirmed by supplemental testing as part of a validated HIV testing algorithm. INTRODUCTION: The Human Immunodeficiency Virus (HIV) is a retrovirus that infects cells of the immune system, destroying or impairing their function. The most advanced stage of HIV infection is Acquired Immunodeficiency Syndrome (AIDS). The general method of detecting infection with HIV is to observe the presence of antibodies to the virus by an EIA method followed by confirmation with any confirmation method. AccuTest HIV – 1/2 Ab is a simple, visual qualitative test that detects antibodies in human serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes. PRINCIPLE: AccuTest HIV – 1/2 Ab employs chromatographic lateral flow device in a cassette format. Colloidal gold conjugated recombinant antigens (Au-Ag) corresponding to HIV-1 (gp120 + gp41) and HIV-2 (gp-36) are dry-immobilized at the end of nitrocellulose membrane strip. HIV-1 & HIV-2 antigens are bound at the Test Zone (1 & 2) respectively. Goat Anti-Mouse IgG antibodies are bound at the Control Zone(C). When the sample is added, it migrates by capillary diffusion rehydrating the gold conjugate. If there are HIV-1 or HIV-2 antibodies in sample, they will bind with the gold conjugated antigens forming particles. These particles will continue to migrate along the strip until the Test Zone (1 or 2) where they are captured by the HIV-1 or HIV-2 antigens generating a visible purple line. If the specimen contains antibodies to HIV-1, the specimen will bind to the 1 test line and produce line. If specimen contains antibodies to HIV2, the specimen will bind to the 2 test line. If there are no HIV-1 or HIV-2 antibodies in sample, no purple line is formed in the Test Zone. The gold conjugate will continue to migrate alone until it is captured in the Control Zone (C) by the Goat Anti Mouse IgG antibodies aggregating in a purple line, which indicates that the migration of liquid has been successful. The control line must be present for the test to be valid. PRECAUTIONS: 1. For best results, adhere to instructions provided. 2. All specimens should be handled as potentially infectious. 3. The test device is sensitive to humidity as well as heat. 4. Do not use beyond expiration date. 5. Do not use test kit if pouch is damaged or seal is broken. 6. Use test device immediately after removing from the pouch. 7. The components (test device and assay diluents) in this kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers. 8. The AccuTest HIV – 1/2 Ab Test devices should be stored at 4 to 30 °C. Do not expose the kit to temperature over 30 °C. 9. Specimen with extremely high concentrations of red blood cells, fibrin should be recentrifuged before use. 10. AccuTest HIV – 1/2 Ab Test Device (Serum/Plasma) is for in vitro diagnostic use only. 11. AccuTest HIV – 1/2 Ab Test Device (Serum/Plasma) will only indicate the presence of antibodies to HIV-1/2 in the specimen and should not be used as the sole criteria for the diagnosis of HIV-1, HIV-2, and/or HIV-1 subtype O infection. 12. For confirmation of reactive test results, specimens should undergo further testing using different assays, such as rapid diagnostic tests, EIA and/or Western blotting in accordance with a validated HIV testing algorithm. 13. As with all diagnostic tests, all results must be interpreted together with other clinical information available to the physician. 14. Results should not be used to determine the serotype of HIV infections TEST PROCEDURE: 1. Allow the test device, buffer and specimen to reach room temperature (15-30 °C) prior to testing. 2. Remove the test device from the foil pouch and use the test device as soon as possible (within one hour). 3. Place the device on a flat, dry surface. Label with specimen ID. 4. Holding the sample dropper vertically above the test disk, slowly transfer 1 drop (10µl) of sample in to the sample well, then add 2 drops of assay diluent (about 75 µl) and start the timer. 5. As the test begins to work, you will see purple color moving across the result Window in the center of the Test Disk. 6. Wait for the colored lines to appear. Interpret test results at 15 to 20 minutes. Do not interpret test result after 20 minutes. STORAGE AND STABILITY Store as packaged in the sealed pouch at 4-30 °C (storage in refrigerator is permitted). Do not store in the freezer. Protect the test kit from humidly. The test device is stable until the expiration date printed on the test kit and/or sealed test device pouch. Do not use beyond the expiration date. The test device must remain in the sealed pouch until use.

Xpress A1c strips are used for a testing of quantitative determination of glycated hemoglobin(HBA1c) in human whole blood. It is used to monitor metabolic control in diabetic patients. it helps in diagnosis of the diabetes or pre-diabetes in adults. Buy Xpress A1c strips online (Pack of 25 Strips) – the best a1c test strips from Point of Care (POC) Range of Accurex HbA1c strips works as both a pipette and measuring element. A Blood drop of 8uL is needed for measurement. This blood is drawn into the cavity by capillary action. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes. The Xpress A1c strips works as both a pipette and measuring element. A Blood drop of 8uL is needed for measurement. This blood is drawn into the cavity by capillary action. The Xpress A1c strips then needs to be inserted into Xpress A1c meter for hemoglobin measurement, The Xpress A1c meter measures the absorbance of whole blood at Hb isosbestic point. Xpress A1c meter uses two wavelengths of light to calculate Hemoglobin level, user level calibration is not required. How to use: Step 1: Wash hands using soap and warm water. Rinse and dry thoroughly. Step 2: Turn on the meter by pressing-releasing the power button. Step 3: Remove an Xpress A1c strip from the vial. Step 4: Prick a finger to obtain a blood sample. Step 5: Touch and hold the drop of blood to the pointed edge of the Xpress A1c strip. The blood is drawn into the Xpress A1c strip by capillary action Step 6: Once the blood fills the Xpress A1c strip chamber. Insert the Xpress A1c strip into the Xpress A1c meter. Step 7: Your Hemoglobin result will appear on the display window. Step 8: Remove the Xpress A1c strip from the meter and discard it. The meter will automatically turn off or long-press the power button to turn off. The Xpress A1c strips are used to quantitatively measure the concentration of HbA1C in whole blood, suitable for the self-monitoring of HbA1C for diabetes patients. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes. is used to quantitatively measure the concentration of HbA1C in whole blood, suitable for the self-monitoring of HbA1C for diabetes patients. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes.Features: Sample Type: Whole Blood/EDTA Blood/Capillary Blood Measuring Range: 0 to 25 g/dl Temperature: 0°C-50°C Storage Temperature: Room Temperature Expiry: Long Expiry(min 02 yrs) Pack Size: 25 Test/Vial LIMITATION AND WARNING: 1. This product is used for In Vitro Diagnostics only, not for in vivo use. 2. This product should not be used past the expiration date. 3. If there is evidence of microbial contamination or browning, discard the vial. 4. This product is not intended to be used as an HbA1c standard. 5. Preservatives contained in the control, rinse with water if splash into the mouth or eyes, and seek medical help as soon as possible. 6. Potential biological risk. Direction for Use This product should be run in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. (1) Dissolution: Open the cap of the vial, and then add 2 drops of Buffer A. Close the cap, and slightly shake the vial until the powder dissolved completely. And please shake it well before using it. (2) Testing in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. Please refer to the B Storage: 1. This product will be stable for 24 months when stored tightly capped at 2-8℃. 2. After dissolved, the product can be stable for 8 hours at 10-30℃, or 5 days at 2-8℃. Do not freeze it. COMPOSITION: This product is prepared from human blood and contains normal hemoglobin, preservatives and stabilizers. The control is provided in lyophilized powder form for increased stability. The kit contains two levels of control, level 1 is with yellow cap, and level 2 is with green cap.