Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Reagents / Reagent Kit / Reagent Kit Enzyme Immunoassay (EIA) Toxoplasma IgM For use with Microwell Reader capable of reading Absorbance at 405 nm / Dual Wave Length Readers are Recommended 96 TestsGSD01-130
Picture of Reagent Kit Enzyme Immunoassay (EIA) Toxoplasma IgM For use with Microwell Reader capable of reading Absorbance at 405 nm / Dual Wave Length Readers are Recommended 96 TestsGSD01-130

Reagent Kit Enzyme Immunoassay (EIA) Toxoplasma IgM For use with Microwell Reader capable of reading Absorbance at 405 nm / Dual Wave Length Readers are Recommended 96 TestsGSD01-130

Reagent-Kit-Enzyme-Immunoassay-(EIA)-Toxoplasma-IgM-For-use-with-Microwell-Reader-capable-of-reading-Absorbance-at-405-nm--Dual-Wave-Length-Readers-are-Recommended-96-TestsGSD01-130

SKU #

#1162985

MPN #

GSD01-130

Brand

Gold Standard Diagnostics Corp

Stock

In Stock

Quantity

100

Features

REAGENT, TOXOPLASMA IGM ANTI-TOXOPLASMA GONDII (96/KT) D/S

$258.28 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1162985
Manufacturer # GSD01-130
Manufacturer Gold Standard Diagnostics Corp
Application Reagent Kit
Container Type Microwell
For Use With For use with Microwell Reader capable of reading Absorbance at 405 nm / Dual Wave Length Readers are Recommended
Number of Tests 96 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Sample Type Human Serum Sample
Storage Requirements Requires Refrigeration
Test Name Toxoplasma IgM
Test Type Enzyme Immunoassay (EIA)
UNSPSC Code 41116010
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  • For the qualitative and quantitative detection of human IgM antibodies to Toxoplasma in human serum by enzyme immunoassay, to aid in the diagnosis of Toxoplasma infection
  • A positive result is presumptive for the detection of anti-Toxoplasma gondii antibodies and presumptive for the diagnosis of acute, recent, or reactivated Toxoplasma gondii infection
  • Patient testing with anti-Toxoplasma gondii IgM antibody assay, must be accompanied by an anti-Toxoplasma gondii IgG antibody assay
  • The assay’s performance characteristics have not been established for neonatal toxoplasmosis diagnosis
  • This assay has not been cleared / approved by the FDA for blood / plasma donor screening
  • For in Vitro Diagnostic Use Only