CAV Ag

CAV Ag

Product catalog summary
Intended Use: The Canine Adenovirus Antigen Rapid Test is a lateral flow immunoassay designed for the qualitative detection of Canine Adenovirus (CAV) antigens in canine eye, nasal fluid, or saliva samples. It aids in determining CAV infection but should not be solely relied upon for a definitive diagnosis.
Reagent and Materials Provided: The kit includes test devices, swabs, buffer tubes, a package insert, and a workstation.
Materials Required but not Provided: A timer is necessary for the procedure.
Storage and Stability: Store the test device at room temperature (4-30℃) away from light. Do not freeze. Use before the expiration date on the package.
Warnings, Precautions, and Safety Information: Handle all samples as potentially infectious. Wear protective gloves and wash hands thoroughly after handling. Dispose of all samples and used kits according to regulations.
Test Procedure: Ensure the kit contents are complete and the test is conducted at room temperature (15–30℃). Collect the specimen using a swab, mix with buffer, and add three drops to 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. An invalid result shows no colored line in the C region.
Limitations: The test is for canine use only. Results may be affected by humidity and temperature. Do not reuse components or mix components from different lots.
Performance Characteristics: The diagnostic sensitivity of the test is 94.94%, specificity is 96.30%, and total agreement is 95.63%.
See more

Catalog excerpts

CAV Ag-1

Canine Adenovirus Antigen Rapid Test(CAV Ag) Intended Use Canine Adenovirus Antigen Rapid Test is a lateral flow immunoassay intended for the qualitative detection of specific antigen from Canine Adenovirus (CAV) in eye, nasal fluid or saliva sample. The test is useful for determination of CAV infection. Reagent and Materials Provided ■ Test devices Materials Required but not Provided Timer Storage and Stability The test device is sealed and should be stored away from light at a room temperature (4-30oC). 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 canine 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—30C) before testing. STEP 2 TEST PROCEDURE Unseal the extraction tube containing the buffer. Place the extraction tube in the workstation. 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 Use the swab to collect secretions specimen from canine eye, nose or mouth. Rotate the swab more than 10 times. Close the cap of the buffer tube. Performance Characteristics Method 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. Invalid: No colored line appears in C region, regardless of T line’s appearance. contains sufficient for <n> tests temperature limitation Limitations Although the Canine Adenovirus Antigen Rapid Test is very accurate in detecting Canine Adenovirus 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.

 Open the catalog to page 1

All Hangzhou Antigenne Technology Co. Ltd catalogs and technical brochures

  1. BVDV Ag

    1  Page

  2. BVDV Ag

    1  Page

  3. BRU Ab

    1  Page

  4. FPV GIA Ag

    1  Page

  5. CDV CPV Ag

    1  Page

  6. CDV CPIV Ag

    1  Page

  7. CDV CAV Ag

    1  Page

  8. FPV FCoV Ag

    1  Page

  9. ICH Ab

    1  Page

  10. HP Ag

    1  Page

  11. GIA Ag

    1  Page

  12. FPL

    1  Page

  13. FHV Ab

    1  Page

  14. FCV Ab

    1  Page

  15. FCoV Ab

    1  Page

  16. F.IgE

    1  Page

  17. F-BT A+B

    1  Page

  18. CRV Ag

    1  Page

  19. C.IgE

    1  Page

  20. C.FOB

    1  Page

  21. BC Ab

    1  Page

  22. FIPV Ag

    1  Page

  23. FeLV Ag

    1  Page

  24. FCoV Ag

    1  Page

  25. F.GIA Ag

    1  Page

  26. RAB Ag

    1  Page

  27. CPV Ab

    1  Page

  28. CIV Ag

    1  Page

  29. CAV-II Ag

    1  Page

  30. CAV-I Ag

    1  Page

  31. SE Ag

    1  Page

  32. BRU Ab

    1  Page

  33. FPV/FCoV Ag

    1  Page

  34. ITGen catalog

    28  Pages

*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.