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Chlamydia pneumoniae EIA tests
MPIN: MP41149
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- Specific antigens
- Internal and external quality monitoring
- Long shelf life even for opened kit components (6 months)
- Higher throughput and objective reading compared to MIF
- Interchangeable reagents and similar procedures
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Highly specific antigens and quality monitoring guarantee accurate resultsConvenient tests suitable for different automatic systems and manual testing.
Benefits
- High accuracy
- Constant quality
- High stability
- Convenient testing
Features
- Specific antigens
- Internal and external quality monitoring
- Long shelf life even for opened kit components (6 months)
- Higher throughput and objective reading compared to MIF
- Interchangeable reagents and similar procedures
Specification
Chlamydia pneumoniae IgG EIA, 96 wells, Cat. 6111300
Chlamydia pneumoniae IgA EIA, 96 wells, Cat. 6111310
Chlamydia pneumoniae IgM EIA, 96 wells, Cat. 6111320
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Neoscreen IRT
Cystic Fibrosis (CF) is an autosomal recessive disorder affecting the lungs, pancreas, intestine and liver. CF is the most common in Caucasians with an incidence rate 1:2500 newborns. CF is caused by mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CTFR) [1,2]. Large-scale neonatal screening for CF is performed by indentification of increased levels of immunoreactive trypsinogen (IRT) in blood.
SKU: MP40991
