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ITEM#: 2013-3305001U
MFR#: 3305-001U
The GSP Neonatal 17?-OH-progesterone assay is intended for the quantitative determination of 17OHP in dried blood spot specimens as an aid in screening newborns for CAH. Congenital adrenal hyperplasia (CAH) is a genetic disorder and the most severe
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
GSP Neonatal 17?-OH-progesterone kit
|
Congenital adrenal hyperplasia (CAH) is a genetic disorder and the most severe form of the disease can lead to a life threatening condition during the first weeks of life. The disease is caused by enzyme defects in steroid biosynthesis, the most fre | 2013-33050010 | EA | |
DELFIA Neonatal 17-OH-progesterone kit (10 plate)
|
DELFIA Neonatal 17-OH-progesterone kit. DELFIA Neonatal 17-OH-progesterone kit is used for the determination of 17a-OH-progesterone on the VICTOR2 D instrument in newborns. | 2013-A024110 | EA | |
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 | |
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 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 |