EHR_ANA Ab
GMP Certified
A Specialized Brand by ITGen

Sabervet Canine Ehrlichia/Anaplasma Antibody Combo Rapid Test

Sabervet’s C.EHR/C.ANA Antibody Combo Rapid Test detects specific antibodies against Ehrlichia and Anaplasma in canine blood samples. It delivers results in 5–10 minutes with high sensitivity and specificity, ideal for tick-borne disease screening.

This lateral flow immunoassay is designed for the qualitative detection of antibodies against Canine Ehrlichia and Anaplasma in serum, plasma, or whole blood. With sensitivities of 98.50% for EHR and 98.13% for ANA, it offers a reliable serological tool for veterinary practices. The test is easy to perform and provides clear results within minutes, supporting […]

Sensitivity
98%
Specificity
97.67%
Reaction Time
5-10 mins
Shelf Life
36 months (when stored unopened at 2–30°C) / Final expiration date is indicated on the package.
Technical Data

Product Parameters

Engineered for precision, built for reliability

Specimen Type
Whole Blood/Serum/Plasma
Detection Method
Lateral Flow Assay
Format
Cassette
Result Time
10 minutes
Sensitivity
98%
Specificity
97.67%
Storage Conditions
2-30°C / 35.6-86°F
Shelf Life
36 months (when stored unopened at 2–30°C) / Final expiration date is indicated on the package.
Packaging
10 Tests/Box
Certifications
CE, ISO 13485 & GMP certified
OEM/ODM Service
Available

Clear Results, Confident Diagnosis

Eliminate diagnostic uncertainty with our advanced colloidal gold technology that delivers crystal-clear test lines and reliable results every time.

SaberVet Advantage

Clear SaberVet test results
  • Deep red, crystal-clear T-lines
  • Clean, interference-free background
  • GMP-controlled batch consistency
  • Confident, reliable diagnosis

Simple 4-Step Protocol

Streamlined workflow for accurate results in minutes

1

Sampling

Collect fecal sample using provided swab

2

Dilution

Mix sample thoroughly in assay buffer tube

3

Loading

Add 3 drops to sample well (S) on test device

4

Interpret

Read results after 5-10 minutes

Scientific Validation

Rigorous testing ensures diagnostic confidence

Clinical Performance vs PCR Gold Standard

Clinical Sensitivity 97.6%
Clinical Specificity 98%
Overall Accuracy 98.8%

Study Details: Comparative analysis conducted on 500 clinical samples across 3 different production lots, ensuring batch-to-batch consistency and reliability.

Complete Kit Components

Everything you need for accurate testing

Test Device

Individual foil pouch with desiccant

Assay Buffer

Pre-measured extraction tube

Disposable Swab

Sterile sampling swab

Instructions

Detailed IFU manual

Work Station

Organized Diagnostic Card Station

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