Veterinary IVD | Colloidal Gold Immunochromatography

E. canis / Anaplasma / Babesia / Leptospira / Lyme Ab Combo Rapid Test

Qualitative differential detection of common vector-borne disease antibodies in blood-derived specimens. Multiplex cassette supports broad tick-borne and infectious disease screening.

25 tests/box 10 min result 2-30°C storage
E. canis / Anaplasma / Babesia / Leptospira / Lyme Ab Combo Rapid Test

Overview

Product Features

Clear C/T line reading

Colloidal gold lateral-flow format supports visual interpretation in clinics, labs and field screening.

Pet-matched specimen workflow

Specimen handling is aligned to the assay type, including feces, swabs, whole blood, serum or plasma.

Distributor-ready pack size

Veterinary rapid tests are configured as 25 tests/box for clinic, channel and batch-testing needs.

Professional IVD presentation

Individually pouched cassettes, buffer and disposable sampling components support storage and traceability.

Professional Kit Configuration

E. canis / Anaplasma / Babesia / Leptospira / Lyme Ab Combo Rapid Test is supplied with matched cassette, buffer and disposable sampling accessories for a controlled veterinary lateral-flow workflow.

Technical Specifications

Intended use Qualitative differential detection of common vector-borne disease antibodies in blood-derived specimens.
Method Colloidal gold immunochromatography
Format Five-panel combo rapid test cassette
Target analyte E. canis, Anaplasma, Babesia, Leptospira and Lyme antibodies
Species Dog / Cat
Specimen Whole blood, serum or plasma
Result time 10 minutes
Storage 2-30°C
Shelf life 24 months
Pack size 25 tests/box
Use Professional veterinary in vitro diagnostic use

Testing Workflow

  1. 1 Collect the validated specimen and mix it thoroughly with assay buffer as instructed.
  2. 2 Apply the processed sample to the cassette sample well using the specified volume or drops.
  3. 3 Read the C/T line result within the defined interpretation window; do not interpret expired reads.

Note

This page is a product overview. Final sample volume, procedure, registered intended use and performance data should follow the package insert and local regulatory requirements.