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The Clostridium difficile Toxin A + Toxin B combination rapid test (Feces) is a rapid chromatographic immunoassay for the qualitative detection of Toxin A and Toxin B Clostridium difficile antigens in human stool samples. The Clostridium difficile Toxin A + Toxin B Combination Rapid Test detects two distinct antigens in stool samples for C. difficile, viz., Toxin A and Toxin B on two different test strips in the same device, thus simultaneously detects two specific Clostridium antigens hard. Clostridium difficile is an anaerobic bacterium that acts as an opportunistic pathogen: it grows in the intestine when the normal flora is altered by antibiotic therapy. Toxigenic strains of Clostridium difficile cause infections from simple diarrhea to pseudomembranous colitis, which can even cause death. The disease is caused by two toxins produced by the toxigenic strains of C. difficile:

FIV Antibody + FeLV Antigen Combo (Whole Blood/Serum/Plasma) is a combined rapid cassette test, capable of separately diagnosing the presence of Feline Immunodeficiency Antibody and Feline Leukemia Virus Antigen in Feline Whole Blood, serum or plasma. FIV Antibody + FeLV Antigen Combo is a lateral flow immunochromatographic rapid cassette test using the direct (or Sandwich) method. The device has two test windows. Each test window has an invisible T (test) zone and C (control) zone. When the sample is applied to the wells (S) on the cassette, the liquid flows sideways on the surface of the test strip. If there is a sufficient amount of Feline immunodeficiency antibody or Feline leukemia virus antigen in the sample, a visible T line will be displayed in the corresponding test window. Line C should always appear after applying a sample, thus indicating that the result is valid.

Test HIV 1.2 – Product code: 90-1015 The Insti Hiv Test for self-diagnostic use is a single-use, vertical scrolling, qualitative immunoassay for the detection of antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2) in whole blood from lancing device. Insti Hiv Test for self-diagnostic use is intended to be used as a test to aid in the diagnosis of HIV-1 and HIV-2 infection using a small drop of blood (50μL) obtained by finger prick. Extensive research studies have shown that this test is extremely accurate when done correctly. It has a proven sensitivity (measure of reliability that the test will be positive for those with HIV infection) of 99.8%. The INSTI HIV-1 / HIV-2 Antibody Test is a qualitative, fast-scrolling, single-use in vitro test for the detection of Human Immunodeficiency Virus Type 1 and Type 2 antibodies on human whole blood collected in EDTA, blood from finger pricker, serum or EDTA plasma.