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ITEM#: 2013-NP4000
MFR#: NP-4000
Neonatal Phenylalanine kits are intended for the quantitative determination of phenylalanine in blood specimens dried on filter paper as an aid in identifying phenylketonuria in newborns. Neonatal Phenylalanine kits are intended for the quantitative
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
GSP Neonatal Phenylalanine kit
|
Phenylketonuria (PKU) is a disorder of amino acid metabolism with reported incidence ranging from 1 in 19,000 to 1 in 13,500 newborn infants*. It is caused by an inability to convert phenylalanine to tyrosine due to deficient activity of the enzyme, | 2013-33080010 | EA | |
Neonatal Phenylalanine kit (10 plate)
|
Neonatal Phenylalanine kits are intended for the quantitative determination of phenylalanine in blood specimens dried on filter paper as an aid in identifying phenylketonuria in newborns. Neonatal Phenylalanine kits are intended for the quantitative | 2013-NP1000 | EA | |
GSP Neonatal IRT kit
|
The GSP Neonatal IRT assay allows the quantitative determination of IRT from dried blood spot specimens, and is intended as an aid in screening for cystic fibrosis. The diagnosis of cystic fibrosis is often based on the symptoms, which may cause co | 2013-3306001U | EA | |
GSP Neonatal hTSH kit
|
Congenital hypothyroidism (CH) results from a failure of the thyroid glands to produce thyroid hormones in adequate amounts. The condition can easily be treated with daily doses of thyroid hormones but clinical diagnosis is difficult to establish an | 2013-33010010 | EA | |
GSP Neonatal Biotinidase kit
|
The GSP Neonatal Biotinidase assay is intended for the quantitative determination of biotinidase activity in blood specimens dried on filter paper as an aid in screening newborns for biotinidase deficiency by using the GSP instrument. The incidence | 2013-3307001U | EA |