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C.LSH Ab
GMP Certified
A Specialized Brand by ITGen

Sabervet Canine Leishmania Antibody Rapid Test

The Sabervet Canine Leishmania Antibody (C.LSH Ab) Rapid Test is a specialized diagnostic tool for the qualitative detection of Leishmania antibodies in dogs. Offering a high total agreement of 98.39%, it supports veterinarians in the early determination of infection. Suitable for serum, plasma, or whole blood samples, this kit provides clear, actionable results on-site in under 10 minutes.

Designed for B2B clinical distribution, the Sabervet C.LSH Ab kit utilizes advanced lateral flow technology to identify specific antibodies against Canine Leishmania. The kit is highly reliable with a diagnostic sensitivity of 98.67% and specificity of 98.13%. It includes everything needed for professional testing: test devices, buffer, quantitative droppers, and a workstation. Its stable storage […]

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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