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Campylobacter Antigen Rapid Test Strip Online Inquiry

Cat#:RTS-046
Product Name:Campylobacter Antigen Rapid Test Strip
Size: 20T
Sample: Stool, Food
Intended use: The Rapid Campylobacter is a rapid chromatographic immunoassay for the qualitative detection of Campylobacter in feces specimens, which might be useful for the diagnosis of campylobacteriosis.
Description: Infection with Escherichia coli O157:H7 (Enterohemorrhagic Escherichia coli) presents with a wide spectrum of clinical manifestations, including asymptomatic carriage, nonbloody diarrhea, hemorrhagic colitis, the hemolytic-uremic syndrome, and thrombotic thrombocytopenic purpura. Not only is E. coli O157:H7 an important agent for hemorrhagic colitis, it is also one of the leading causes of bacterial diarrhea. Transmission of E. coli O157:H7 is primarily food-borne. Undercooked meat is the most common culprit, dairy products and secondary person-to-person spread are also important. The organism produces at least two Shiga-like toxins. These toxins are thought to have direct pathogenic significance in E. coli O157:H7 infection. This infection is usually diagnosed from a positive stool culture, from the presence of Shiga toxins, or both. Timely collection (within 7 days of illness onset) of a stool sample for culture is imperative for a high recovery rate.
Detection Principle: The Rapid Campylobacter is a qualitative lateral flow immunoassay for the determination of Campylobacter in feces samples. The membrane is pre-coated with monoclonal antibodies against Campylobacter antigens on the test line region. During testing, the sa
Contents of Kit: 1. Card tests 2. Instructions for use 3. Specimen collection vial with buffer
Sensitivity: Sensitivity: >99% and specificity 98%.
Storage: Store at 15-25℃, DO NOT FREEZE or use beyond the expiration date. The shelf life is 36 months.
References: 1. Kawatsu, K. et al. “Development and Evaluation of Immunochromatographic Assay for Simple and Rapid Detection of Campylobacter jejuni and Campylobacter coli in Human Stool Specimens”. Journal of Clinical Microbiology Apr. 2008 Vol 46, No. 4, p. 1226- 12

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