BIONOTE Anigen Rapid CaniV-4 – 4-in-1 Canine Vector-Borne Disease Test – 10 Tests
Description The BIONOTE Anigen Rapid CaniV-4 Test Kit is a veterinary rapid diagnostic test designed for the simultaneous detection of four important canine vector-borne disease markers. Using an immunochromatographic assay, the test detects: Dirofilaria immitis antigen — Heartworm Ehrlichia canis antibody — Ehrlichiosis Borrelia burgdorferi antibody — Lyme disease Anaplasma phagocytophilum / Anaplasma platys antibodies — Anaplasmosis The test can be performed using canine whole blood, serum, or plasma, making it suitable for veterinary clinics and diagnostic screening. Its four-target format allows veterinarians to screen for multiple vector-borne disease markers using a single test device, helping streamline routine canine diagnostic workups. Key Features 4-in-1 canine vector-borne disease screening Detects Heartworm, Ehrlichia, Lyme disease, and Anaplasma markers Simultaneous detection of four targets Rapid immunochromatographic test Suitable for canine whole blood, serum, or plasma Easy visual result interpretation No dedicated analyzer required 10 tests per kit Storage at 2–30°C Designed for veterinary diagnostic use What Does It Detect? Target Marker Detected Disease / Condition Dirofilaria immitis Antigen Heartworm disease Ehrlichia canis Antibody Canine ehrlichiosis Borrelia burgdorferi Antibody Lyme disease Anaplasma phagocytophilum / A. platys Antibody Canine anaplasmosis Important: The Anaplasma component detects antibodies to A. phagocytophilum and/or A. platys and does not differentiate between the two species. Product Specifications Specification Details Brand BIONOTE Product Name Anigen Rapid CaniV-4 Product No. RC2120DD Test Type 4-in-1 canine vector-borne disease test Method Chromatographic / immunochromatographic assay Animal Dog Specimens Whole blood, serum, plasma Targets D. immitis Ag, E. canis Ab, B. burgdorferi Ab, Anaplasma Ab Testing Time Approximately 15 minutes Pack Size 10 Tests/Kit Storage 2–30°C Intended Use Veterinary diagnostic use BIONOTE's current product page lists RC2120DD, 10 Tests/Kit, and storage at 2–30°C. BIONOTE's product catalog lists the standard CaniV-4 testing time as 15 minutes. Sample Types The test can be used with: Canine whole blood Canine serum Canine plasma For whole blood, the manufacturer's IFU specifies using the supplied anticoagulant tube. General Test Procedure Collect the appropriate canine blood sample. Add 20 µL of whole blood, or 10 µL of serum/plasma, to the sample hole using the appropriate supplied capillary tube or micropipette. Add 2 drops of assay diluent. Allow the sample to migrate through the test window. Interpret the results at approximately 15 minutes. Do not interpret results outside the manufacturer's specified reading time. Result Interpretation The test contains control and test lines for the different disease markers. Negative: Only the appropriate control line appears for the tested area. Positive: The control line and corresponding test line appear, indicating detection of the respective antigen or antibody. Invalid: If the required control line does not appear, the result is invalid and the test should be repeated using a new device. A positive antibody result indicates the presence of antibodies and should be interpreted together with the dog's clinical history and other laboratory findings. Kit Contents For the 10 Tests/Kit configuration, the manufacturer's IFU lists: 10 × Anigen Rapid CaniV-4 test devices Assay diluent 10 × anticoagulant tubes 10 × disposable capillary tubes Instructions for Use Storage & Handling Store at 2–30°C Do not freeze Keep away from excessive heat and humidity Remove the test device from the foil pouch immediately before use Do not reuse test components Check the expiration date before use Follow the manufacturer's current Instructions for Use Important Diagnostic Note CaniV-4 is a screening/diagnostic aid, and results should not be used as the sole basis for a definitive clinical diagnosis. BIONOTE's IFU notes that questionable results may require additional clinical and/or laboratory testing and that final diagnosis should be made by a veterinarian after evaluating all relevant findings.
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