FPV/FCoV Ag

FPV/FCoV Ag

Product catalog summary
Intended Use: The Feline Panleukopenia Virus/Coronavirus Antigen Combo Rapid Test is a lateral flow immunoassay designed for the simultaneous qualitative detection of antigens from Feline Panleukopenia Virus (FPV) and Feline Coronavirus (FCoV) in fresh feces or rectal swab samples. It aids in determining FPV and FCoV infections.
Reagent and Materials Provided: The kit includes test devices, swabs, buffer tubes, a workstation, and a package insert.
Materials Required but not Provided: A timer is needed to read the results accurately.
Storage and Stability: The test device should be stored at room temperature (4-30℃) away from light and should not be frozen. It must be used before the expiration date on the package label.
Warnings, Precautions, and Safety Information: The test is for feline use only. Results can be affected by humidity and temperature. Ensure the foil pouch is undamaged before opening and use the test immediately after opening. Do not reuse components or use them after expiry. Do not mix components from different lots. Handle all samples as potentially infectious, wearing protective gloves and disposing of materials safely according to regulations.
Test Procedure: Collect a fresh fecal sample using the swab, place it in the buffer tube, and rotate the swab more than 10 times. Add three drops of the mixed sample into the specimen well of the test device. Read results at 5-10 minutes; results are invalid after 15 minutes.
Interpretation of Test Results: A negative result shows only a clear C line. A positive result shows both C and T lines, regardless of the T line's intensity. An invalid result shows no colored line in the C region.
Performance Characteristics: For FCoV Ag, diagnostic sensitivity is 98.50%, specificity is 97.33%, and total agreement is 98.00%. For FPV Ag, diagnostic sensitivity is 98.00%, specificity is 97.50%, and total agreement is 97.71%.
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Catalog excerpts

FPV/FCoV Ag-1

Feline Panleukopenia Virus/ Coronavirus Antigen Combo Rapid Test(FPV/FCoV Ag) Feline Panleukopenia Virus/Coronavirus Antigen Combo Rapid Test is a lateral flow immunoassay intended for the simultaneous qualitative detection of specific antigen from Feline Panleukopenia Virus (FPV) and Feline Coronavirus (FCoV) in fresh feces or rectal swab sample. The test is useful for simultaneous determination of FPV and FCoV infection. Reagent and Materials Provided • Test devices • Swabs • Buffer tubes • Package insert Materials Required but not Provided The test device is sealed and should be stored away from light at a room temperature (4-30C). Do not freeze. The test device should be used before the expiration date marked on the package label. Warnings, Precautions and Safety Information 1. The test device is used for feline only. 2. The results may be influenced by humidity and temperature. 3. Make sure that the foil pouch containing the test is not damaged before open. Perform the test immediately when the pouch package is opened. 4. Do not reuse the test components. 5. Do not use after the expiry date. 6. Do not mix product components in different lot numbers. 7. As all samples are potentially infectious. Operators should wear protective gloves while handling samples and wash hands thoroughly afterwards. 8. Decontaminate and dispose of all samples, used kits and potentially contaminated materials safely in accordance with national and local regulations. STEP 1 CHECK THE KIT CONTENTS BEFORE USE Check the product contents and make sure the test operation is under the room temperature (15—30oC) before testing. STEP 2 TEST PROCEDURE Performance Characteristics Take the test device out of the aluminum foil bag and place it on a clean and flat table. Add three drops (about 90 pL) of specimen (mixed sample) vertically into the specimen well (S) of the test device. STEP 3 INTERPRETATION OF TEST RESULT Read the result at 5-10 minutes. The result is invalid after 15 minutes. Positive (+): The presence of both C line and T line, regardless of T line being strong or faint. Negative (-): Only clear C line appears. Unseal the extraction tube containing the buffer. Place the extraction tube in the workstation. Use the swab to collect some fresh feline feces or fecal sample from its rectum. And then put the swab into the buffer. Close the cap of the buffer tube. Invalid: No colored line appears in C region, regardless of T line’s appearance. Although the Feline Panleukopenia Virus/Coronavirus Antigen Combo Rapid Test is very accurate in detecting Feline Panleukopenia Virus Antigen and Feline Coronavirus Antigen, a low incidence of false results may be occurred. Other clinically or laboratory tests might be required if questionable results are obtained. As other diagnostic tests, a definitive clinical diagnosis should not be based on the result of a single test, but should be diagnosed by the veterinarian after all clinical and laboratory findings have been evaluated. Diagnostic Sensitivity of FCoV Ag: 197/200=98.50%(95%CI* (95.48%-99.69%)) Diagnostic Specificity of FCoV Ag: 146/150=97.33%(95%CI* (93.11%-99.19%)) Total Agreement of FCoV Ag: 343/350=98.00%(95%CI* (95.85%-99.11%)) batch code contains sufficient for <n> tests temperature limitation

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