PAH rabbit pAb
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PAH rabbit pAb
Background :
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]Description :
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],UniProt :
P00439Swiss Prot :
P00439Reactivity :
Human; Mouse; RatImmunogen :
The antiserum was produced against synthesized peptide derived from human PAH. AA range:351-400Clonality :
PolyclonalSource :
RabbitApplications :
WB; IHC; IF; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.Molecular Weight :
51kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
51kDFragment :
IgGSubcellular Location :
Cytosol, extracellular exosomeOther Product Names :
PAH; Phenylalanine-4-hydroxylase; PAH; Phe-4-monooxygenaseGene ID (Human) :
5053

