Feline Panleucopenia Virus Antigen (FPV Ag) Test, Feces/Vomit as specimen,with high specificity

FPV Antigen Rapid Test Cassette is a lateral flow immunochromatographic assay for the qualitative detection of Feline Panleucopenia Virus (FPV Ag) in cat’s feces or vomit.

Feline panleukopenia virus (FPV) infects all felids as well as raccoons, mink and foxes. This pathogen may survive in the environment for several months and is highly resistant to some disinfectants.

FPV Antigen Rapid Test Cassette is a lateral flow immunochromatographic assay based on sandwich ​format. The test cassette has a testing window. The testing window has T (test) region and C (control) region. During testing, sample is applied into the sample well on the cassette. FPV antigens, if present in specimen, react with anti-FPV antibodies coated colloidal gold particles in the test strip. The mixture then migrates upward on the membrane chromatographically by capillary action and reacts with anti-FPV antibodies on the membrane in the test line region. If the specimen contains Feline Panleucopenia Virus, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain FPV antigens, a colored line will not appear in the test line region indicating a negative result. To serve as a procedural 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.

• Remove the test cassette from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour.
• Collect cat’s feces or vomit with the swab from cat’s anus or on the ground. The amount of fecal swab as follows:
• Insert the wet swab into the provided assay buffer tube. Agitate it to assure good sample extraction.

• Place the test cassette on a clean and level surface. Hold

• the dropper vertically and transfer 3 drops of extracted sample (approximately 120 μl) to the specimen well (S) of the test cassette, then start the timer. See illustration below.
• Read the result at 5 minutes. Do not interpret results after 10 minutes.
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CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies.

CITEST manufactures its IVD products in ISO13485:2016 accredited manufacturing facilities under strict quality assurance systems. Our innovative products are developed using industry-leading design control systems, which ensures consistent product quality and performance.

Our products are used in the clinical market to help people live more healthy lives. When you select CITEST products, you can be assured of high performance and accuracy along with a dedicated customer support team.