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Neonatal Phenylalanine
MPIN: MP41073
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Labsystems Diagnostics’ Neonatal Phenylalanine is a chemical method, with fluorometric detection, for quantitative determination of phenylalanine from blood specimens dried on filter paper, intended for newborn screening for phenylketonuria (PKU).
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Labsystems Diagnostics’ Neonatal Phenylalanine is a chemical method, with fluorometric detection, for quantitative determination of phenylalanine from blood specimens dried on filter paper, intended for newborn screening for phenylketonuria (PKU).
Benefits
- Simple and easy to perform
- Excellent analytical sensitivity
- Extensive experiences from worldwide customers
- Calibrated against the latest international references
Specification
Neonatal Phenylalanine 10 solid plates (96) 960 wells 6199896
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Cancellation / Return / Exchange Policy
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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
