CDV CPV Ag

CDV CPV Ag

Product catalog summary
Overview: The Canine Distemper Virus/Parvovirus Antigen Combo Rapid Test is a lateral flow immunoassay designed for the qualitative detection of Canine Distemper Virus (CDV) in eye, nasal fluid, or saliva samples, and Canine Parvovirus (CPV) in fresh feces or rectal swab samples. It aids in determining CDV or CPV infections in canines.
Intended Use: This test is intended for use in veterinary settings to detect CDV and CPV antigens in canine samples.
Reagents 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 needed to perform the test.
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 and Precautions: Handle all samples as potentially infectious. Wear protective gloves and wash hands thoroughly after handling. Dispose of all samples and used materials safely according to regulations.
Test Procedure:
  • Check kit contents and ensure room temperature (15–30℃) before testing.
  • For CDV: Collect secretions from the eye, nasal fluid, or saliva using a swab, then place the swab in the buffer.
  • For CPV: Collect fresh feces or a fecal sample from the rectum using a swab, then place the swab in the buffer.
  • Rotate the swab more than 10 times in the buffer, then close the cap.
  • Place the test device on a flat surface, add three drops (about 90 μl) of the mixed sample into each specimen well.
  • Read the result at 5-10 minutes. Results are invalid after 15 minutes.
Interpretation of Test Results:
  • Positive: Both C line and T line appear, regardless of T line intensity.
  • Negative: Only a clear C line appears.
  • Invalid: No colored line appears in the C region.
Limitations: While the test is accurate, false results may occur. Additional clinical or laboratory tests may be required for confirmation. A definitive diagnosis should be made by a veterinarian after evaluating all clinical and laboratory findings.
Performance Characteristics: The test's performance was evaluated using PCR as a reference method, showing high accuracy in detecting CDV and CPV antigens.
Additional Notes:
  • The test is for canine use only.
  • Results may be affected by humidity and temperature.
  • Ensure the foil pouch is undamaged before opening and perform the test immediately after opening.
  • Do not reuse test components or use them after the expiry date.
  • Do not mix components from different lot numbers.
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Catalog excerpts

CDV CPV Ag-1

Canine Distemper Virus /Parvovirus Antigen Combo Rapid Test (CDV /CPV Ag) Intended Use Canine Distemper Virus /Parvovirus Antigen Combo Rapid Test is a lateral flow immunoassay intended for the qualitative detection of specific antigen from Canine Distemper Virus (CDV) in eye,nasal fluid or saliva sample and Canine Parvovirus (CPV) in fresh feces or rectal swab sample. The test is useful for determination of CDV or CPV infection. Reagent and Materials Provided • Test devices • Swabs • Buffer tubes • Package insert 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 (4-30C). 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 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 “oh? step 3 interpretation of test result Take the test device out of the aluminum foil bag, and place it on a clean and flat table. Add three drops (about 90 ql) of specimen (mixed sample) vertically into the each specimen well (S) of the test device. Read the result at 5-10 minutes. The result is invalid after 15 minutes. @© STEP 2 TEST PROCEDURE CPV Ag Positive (+): The presence of both C line and T line, regardless of T line being strong or faint. Check the product contents and make sure the test operation is under the room temperature (15—30°C) before testing. STEP 2 TEST PROCEDURE CDV Ag tro 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 secretions specimen from canine eye, nasal fluid, or saliva. Then, put the swab into the buffer. 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 Close the cap of the than 10 times. buffer tube. Invalid: No colored line appears in C region, regardless of T line’s appearance. Limitations Although the Canine Distemper Virus / Parvovirus Antigen Combo Rapid Test(CDV/CPV Ag) is very accurate in detecting Canine Distemper Virus / Canine Parvovirus 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. Performance Characteristics 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 ql) of specimen (mixed sample) vertically into the each specimen well (S) of the test device.

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