PAH Polyclonal Antibody
Product Specifications
Background
Phenylalanine hydroxylase (PAH) Homo sapiens 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]
Product Name Alternative
PAH; Phenylalanine-4-hydroxylase; PAH; Phe-4-monooxygenase
Gene ID
5053
Swiss Prot
P00439
Cross Reactivity
Human; Mouse; Rat
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC-p; IF (paraffin section) ; ELISA
Dilution
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
Buffer
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Molecular Weight
51
Storage Conditions
-20°C/1 year
Protein Weight
51
Available Sizes
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