Phenylalanine Hydroxylase ELISA试剂盒
(Phenylalanine Hydroxylase)
PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Jul 2008].
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8 results
适用: 人
Colorimetric
Sandwich ELISA
78.125 pg/mL - 5000 pg/mL
Plasma, Serum, Tissue Homogenate
1 image
适用: 小鼠
Colorimetric
Sandwich ELISA
23.5 pg/mL - 1500 pg/mL
Cell Lysate, Plasma, Serum, Tissue Homogenate
1 image
适用: 小鼠
Colorimetric
Sandwich ELISA
0.31 ng/mL - 20 ng/mL
Cell Lysate, Tissue Homogenate
1 image
适用: 化学剂
Colorimetric
Sandwich ELISA
Plasma, Serum, Tissue Homogenate
Latest Publications for our Phenylalanine Hydroxylase ELISA试剂盒
: "Three novel variants (p.Glu178Lys, p.Val245Met, p.Ser250Phe) of the phenylalanine hydroxylase (PAH) gene impair protein expression and function in vitro." in: Gene, Vol. 668, pp. 135-139, (2018) (PubMed).Aliases for Phenylalanine Hydroxylase ELISA试剂盒
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