Exotic Pets | Reptile Colloidal Gold Rapid Test

Reptile Salmonella Ag Rapid Test Kit

For qualitative detection of Salmonella antigen in reptile feces or cloacal swab specimens to support rapid gastrointestinal bacterial pathogen screening.

10 Tests/Kit 10 minutes 2-30°C Colloidal gold immunochromatography
Reptile Salmonella Ag Rapid Test Kit

Overview

Caratteristiche del prodotto

Rapid screening for reptile gastrointestinal targets

Built for veterinary, laboratory and field screening workflows in turtles, lizards, snakes and other IFU-covered reptiles.

Feces / cloacal swab workflow

Matches practical reptile sampling needs for clinic and husbandry-management scenarios.

Visual C/T line reading

The colloidal gold lateral-flow format can be interpreted within the defined reading window.

10 Tests/Kit channel-ready packaging

Aligned with Safheal companion-animal rapid test packaging for stocking and distribution.

Professional Kit Configuration

Individually pouched cassette, sample extraction tube, disposable swab/sampling accessories and IFU.

Specifications

Uso previsto For qualitative detection of Salmonella antigen in reptile feces or cloacal swab specimens to support rapid gastrointestinal bacterial pathogen screening.
Metodo Colloidal gold immunochromatography
Formato Rapid test cassette
Target analyte Salmonella antigen
Species Reptiles covered by the IFU
Campione Feces / cloacal swab
Result time 10 minutes
Conservazione 2-30°C
Formatoo confezione 10 Tests/Kit
Componenti principali Individually pouched cassette, sample extraction tube, disposable swab/sampling accessories and IFU
Use Professional veterinary in vitro diagnostic use

Testing Procedura

  1. 1 Collect fresh feces or a cloacal swab specimen and mix it with sample buffer as instructed in the IFU.
  2. 2 Apply the specified volume or drops of processed specimen to the cassette sample well.
  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 specimen volume, procedure, registered intended use and performance data should follow the package insert and local regulatory requirements.