Diagnosing a companion animal's disease rapidly and accurately is
what makes both people and animals happy.
Canine Feline Influenza V Ag Test Kit
[CGM-VIG-11] & [CGM-VIG-12]
The RIDX® Canine Feline Influenza V Ag Test Kit is a lateral flow chromatographic immunoassay for the qualitative detection of canine and feline influenza viral antigens in canine and feline pharyngeal or nasal secretions.
This kit shows two letters which are the test (T) line and the control (C) line on the surface of the device.
If the Influenza A virus (IAV) antigens exist in the sample, it binds to the cellulose nanobeads (CNB)-conjugated IAV antibody. The antigen-antibody complex moves through the membrane by capillary force and responds to the IAV antibody on the test line, resulting in a red line. The control line indicates that the test is performed correctly and should appear when the test is complete.
The highly selective and sensitive two monoclonal antibodies to IAV are used as capture and detector in the kit. The RIDX® Canine Feline Influenza V Ag Test Kit can detect IAV H3 and H5 subtype antigens in canine and feline nasal or pharyngeal secretions with high accuracy.
Canine or feline nasal swab or pharyngeal swab
• RIDX CF IAV test device (10 or 2 tests)
• Sample dilution buffer (10 or 2 vials)
• Disposable swab (10 or 2 ea)
• Dropper cap with sample filter (10 or 2 ea)
• Instructions for use (1 sheet)
[For Canine Influenza A Virus]
• Sensitivity: 91.67% (11/12) vs. RT-PCR
• Specificity: 99.21% (125/126) vs. RT-PCR
• Diagnostic Agreements: 98.55% (136/138) vs. RT-PCR
• Limit of Detection: 5 x 103 TCID50/mL for canine IAV H3N2
• No cross-reactivity with other canine pathogens (CCV, CDV, CPV, Escherichia coli, and Giardia spp.)
[For Feline Influenza A Virus]
• Sensitivity: 90.91% (10/11) vs. RT-PCR
• Specificity: 99.12% (113/114) vs. RT-PCR
• Diagnostic Agreements: 98.40% (123/125) vs. RT-PCR
• Limit of Detection: 5 x 103 TCID50/mL for feline IAV H5N1
• No cross-reactivity with other feline pathogens (FCV, FCoV, FPV, Escherichia coli, and Giardia spp.)
• 10 Tests/Kit [CGM-VIG-11]
• 2 Tests/Kit [CGM-VIG-12]
1. All reagents and samples must be at room temperature (15~30℃/59~86℉) before use.
2. Collect nasal or pharyngeal samples using a swab.
3. Put the swab into the sample dilution buffer and stir the solution to disperse the sample into the buffer (approximately 10 seconds).
4. Break the head of the cotton swab and discard the rod.
5. Attach a dropper cap with a filter to the top of the buffer.
6. Apply 4 drops of the sample solution in the sample hole on the device.
7. Read test results at 15 minutes.