ITGen Canine Parvovirus Antigen Rapid Test
The ITGen Canine Parvovirus Antigen Rapid Test uses colloidal gold immunochromatography to capture CPV antigens in fecal samples through specific antibodies and complete the test within 10 minutes. It is suitable for scenarios such as pet hospitals, breeding bases and epidemiological monitoring, especially when dogs have typical symptoms such as bloody diarr
Product Parameters Production Name ITGen Canine Parvovirus Antigen Rapid Test Target Analyte Canine Parvovirus Antigen Specimen Type fresh feces or rectal swab sample Storage Temperature 4-30°C Result Time 5-10 Minutes Packaging Individually Sealed Tests Packaging Specification 10T Shelf Life Up to Expiration Date Indicated on Package Product Specifications Sensitivity 98% Accuracy 98.33% Format Cassette Detection Method Chromatographic Immunoassay/Lateral Flow Immunoassay Specificity 98.67% Reading Time 5-10 Minutes Usage Veterinary Diagnostics Contents Contents Number Test device 1 Swab 1 Buffer tube 1 Package insert 1 Description The project development is aimed at responding to the characteristics of canine parvovirus infection, which has a short incubation period and rapid progression of the disease, improving the efficiency of early identification, and effectively responding to the clinical needs of canine parvovirus, which is highly contagious and has a high mortality rate.
The virus mainly infects puppies and spreads rapidly, and early diagnosis is crucial for treatmenta. How to use? Check the product contents and make sure the test operation is under the room temperature (15–30℃) before testing. Unseal the extraction tube containing the buffer.Place the extraction tube in the workstation.
Use the swab to collect some fresh canine feces or fecal sample from its rectum. And then put the swab into the buffer. Rotate the swab more than 10 times.Close the cap of the buffer tube. Take the test device out of the aluminum foil bag and place it on a clean and flat table.
Add three drops (about 90 μL) of specimen (mixed sample) vertically into the specimen well(S) of the test device. INTERPRETATION OF RESULTS Positive (+): The presence of both C line and T line, regardless of T line being strong or faint. Negative (-): Only clear C line appears. Invalid: No colored line appears in C region, regardless of T line’s appearance.
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