3750 – Anti-GP2 IgA

Highlights

• Use of recombinant human glycoprotein 2 (GP2)
• Ready-to-use (exception: conjugate and wash buffer) and barcoded reagents
• Quality assured handling in routine laboratories
• Incubation at room temperature
• Quantitative determination of IgA antibodies against GP2
• Calibrated with the international standard preparation NIBSC code 08/204
• Results expressed in IU/L
• Excellent diagnostic sensitivity and specificity
• High precision within the measurement range
• CE marked
• Automatable


Intended Purpose

The Anti-GP2 IgA is a quantitative immunoassay for the determination of IgA antibodies against glycoprotein 2 (GP2) in human serum. The Anti-GP2 IgA is intended as an aid in the diagnosis of Crohn’s disease in conjunction with other clinical and laboratory findings. The immunoassay is designed for manual professional in vitro diagnostic use.


Diagnostic Relevance

Non-specific inflammatory bowel diseases, including Crohn’s disease (CD, enteritis regionalis) and ulcerative colitis (UC), involve chronic relapsing inflammatory processes of the intestine. Immunologic, genetic, infectious, and environmental factors contribute to the risk of developing these diseases. Researchers identified autoantibodies of the exocrine pancreas (PAB) as specific serological markers for CD. Membrane-bound pancreatic glycoprotein 2 (GP2) represents the major target of PAB. In combination with the detection of autoantibodies to Saccharomyces cerevisiae (ASCA), which occur in approximately 70% of CD patients, and atypical antineutrophil cytoplasmic antibodies (aANCA), mainly detected in UC patients, PAB against GP2 serve as highly specific serological markers for differentiating CD from UC.

Publications

Product Specifications

Title Anti-GP2 IgA
Product code 3750
Indication Crohn’s disease
Description Enzyme immunoassay for the quantitative determination of IgA antibodies against glycoprotein 2 (GP2) in human serum
Format Microtiter plate coated with recombinant human glycoprotein 2
Total incubation time 105 min.
Sample volume 10 µL serum
No. of determinations 96 (89 x 1) + 5 x Calibrators and 2 x Controls

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Current version of the instructions for use. The respective valid version for processing the test can be found in the product packaging.