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OnSite™ Leishmania Ab Rapid Test Kit, CE, 50 Tests (Strips)

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SKU: R0122S
Brand: CTK Biotech
UoM: Unità
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Store Availability & Pickup
LabMart Limited - Tamale
NS-246, Via, 4388 Tamale-Kumbungu Rd, Tamale, Northern Region, Ghana
Not available
LabMart Limited
10 Rcecourse street, Accra, Greater Accra Region, Ghana
5 available
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MOQ : 1.0 Unità
Estimated delivery Estimated delivery: 3-5 business days
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The OnSite Leishmania Ab Rapid Test CE is a lateral flow immunoassay designed for the qualitative detection of IgG and IgM antibodies to Leishmania donovani (L. donovani), the protozoan responsible for visceral leishmaniasis (kala-azar). This rapid test provides a reliable, cost-effective, and equipment-free diagnostic solution, making it ideal for use in both clinical laboratories and field settings.

The assay employs the recombinant rK39 antigen, a well-characterized marker that ensures high sensitivity and specificity for visceral leishmaniasis detection.

Key Features

  • Detects both IgG and IgM antibodies to L. donovani.
  • Utilizes rK39 antigen for improved accuracy.
  • Simple and rapid procedure requiring no equipment.
  • Individually sealed foil pouches for extended shelf life and reliability.
  • Suitable for serum and plasma specimens.

Kit Contents

Each kit (50 tests) contains:

  • One strip device (per pouch).
  • One desiccant.
  • 5 µL capillary tubes.
  • Sample diluent (REF SB-R0122, 5 mL/bottle).
  • Package insert (instructions for use).

Specifications

ParameterDetails
Product NameLeishmania Ab Rapid Test CE
Catalog NumberR0122S
Format50 tests/kit
Specimen TypeSerum (S), Plasma (P)
DetectionIgG and IgM antibodies to Leishmania donovani
PrincipleLateral Flow Chromatographic Immunoassay
Antigen UsedrK39 recombinant antigen
Turnaround TimeResults within minutes
PackagingIndividually sealed foil pouches with desiccant
External ControlsAvailable separately
Regulatory StatusCE-marked

Applications

  • Rapid screening for visceral leishmaniasis (kala-azar).
  • Epidemiological surveillance of L. donovani infections.
  • Diagnostic support in hospitals, clinics, and field missions.
  • Useful for NGOs and humanitarian health programs in endemic regions.


The OnSite Leishmania Ab Rapid Test CE is a sensitive, specific, and user-friendly diagnostic tool for the detection of antibodies against Leishmania donovani. By utilizing rK39 antigen technology, this CE-marked rapid test ensures accuracy in both clinical and field environments, making it a valuable resource for leishmaniasis diagnosis, surveillance, and control programs worldwide.

Application: Diagnostic Testing
Storage Temperature: Room Temperature
Product Type: Test Kit
Product Brand: CTK Biotech
Product Grade: Medical grade

The OnSite Leishmania Ab Rapid Test CE is a lateral flow immunoassay designed for the qualitative detection of IgG and IgM antibodies to Leishmania donovani (L. donovani), the protozoan responsible for visceral leishmaniasis (kala-azar). This rapid test provides a reliable, cost-effective, and equipment-free diagnostic solution, making it ideal for use in both clinical laboratories and field settings.

The assay employs the recombinant rK39 antigen, a well-characterized marker that ensures high sensitivity and specificity for visceral leishmaniasis detection.

Key Features

  • Detects both IgG and IgM antibodies to L. donovani.
  • Utilizes rK39 antigen for improved accuracy.
  • Simple and rapid procedure requiring no equipment.
  • Individually sealed foil pouches for extended shelf life and reliability.
  • Suitable for serum and plasma specimens.

Kit Contents

Each kit (50 tests) contains:

  • One strip device (per pouch).
  • One desiccant.
  • 5 µL capillary tubes.
  • Sample diluent (REF SB-R0122, 5 mL/bottle).
  • Package insert (instructions for use).

Specifications

ParameterDetails
Product NameLeishmania Ab Rapid Test CE
Catalog NumberR0122S
Format50 tests/kit
Specimen TypeSerum (S), Plasma (P)
DetectionIgG and IgM antibodies to Leishmania donovani
PrincipleLateral Flow Chromatographic Immunoassay
Antigen UsedrK39 recombinant antigen
Turnaround TimeResults within minutes
PackagingIndividually sealed foil pouches with desiccant
External ControlsAvailable separately
Regulatory StatusCE-marked

Applications

  • Rapid screening for visceral leishmaniasis (kala-azar).
  • Epidemiological surveillance of L. donovani infections.
  • Diagnostic support in hospitals, clinics, and field missions.
  • Useful for NGOs and humanitarian health programs in endemic regions.


The OnSite Leishmania Ab Rapid Test CE is a sensitive, specific, and user-friendly diagnostic tool for the detection of antibodies against Leishmania donovani. By utilizing rK39 antigen technology, this CE-marked rapid test ensures accuracy in both clinical and field environments, making it a valuable resource for leishmaniasis diagnosis, surveillance, and control programs worldwide.

No resources are currently available for this product.

This will display Shipping & Return.

The OnSite Leishmania Ab Rapid Test CE is a lateral flow immunoassay designed for the qualitative detection of IgG and IgM antibodies to Leishmania donovani (L. donovani), the protozoan responsible for visceral leishmaniasis (kala-azar). This rapid test provides a reliable, cost-effective, and equipment-free diagnostic solution, making it ideal for use in both clinical laboratories and field settings.

The assay employs the recombinant rK39 antigen, a well-characterized marker that ensures high sensitivity and specificity for visceral leishmaniasis detection.

Key Features

  • Detects both IgG and IgM antibodies to L. donovani.
  • Utilizes rK39 antigen for improved accuracy.
  • Simple and rapid procedure requiring no equipment.
  • Individually sealed foil pouches for extended shelf life and reliability.
  • Suitable for serum and plasma specimens.

Kit Contents

Each kit (50 tests) contains:

  • One strip device (per pouch).
  • One desiccant.
  • 5 µL capillary tubes.
  • Sample diluent (REF SB-R0122, 5 mL/bottle).
  • Package insert (instructions for use).

Specifications

ParameterDetails
Product NameLeishmania Ab Rapid Test CE
Catalog NumberR0122S
Format50 tests/kit
Specimen TypeSerum (S), Plasma (P)
DetectionIgG and IgM antibodies to Leishmania donovani
PrincipleLateral Flow Chromatographic Immunoassay
Antigen UsedrK39 recombinant antigen
Turnaround TimeResults within minutes
PackagingIndividually sealed foil pouches with desiccant
External ControlsAvailable separately
Regulatory StatusCE-marked

Applications

  • Rapid screening for visceral leishmaniasis (kala-azar).
  • Epidemiological surveillance of L. donovani infections.
  • Diagnostic support in hospitals, clinics, and field missions.
  • Useful for NGOs and humanitarian health programs in endemic regions.


The OnSite Leishmania Ab Rapid Test CE is a sensitive, specific, and user-friendly diagnostic tool for the detection of antibodies against Leishmania donovani. By utilizing rK39 antigen technology, this CE-marked rapid test ensures accuracy in both clinical and field environments, making it a valuable resource for leishmaniasis diagnosis, surveillance, and control programs worldwide.

No resources are currently available for this product.

This will display Shipping & Return.