Human PAH (Phenylalanine-4-Hydroxylase) - Recombinant Protein

Name: Human PAH (Phenylalanine-4-Hydroxylase) - Recombinant Protein
Brand: Astor Scientific
SKU: ASTP1509
Price: 429.99 USD
Availability: InStock

Molecule: PAH
Species: Human
Expression System: E.coli
Tag: N-6His
Expression Range: 1-226aa

$429.99 ~~$549.99~~

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Astor Scientific

Human PAH (Phenylalanine-4-Hydroxylase) - Recombinant Protein

$429.99 ~~$549.99~~

Product Overview

Product Name	Recombinant Human Phenylalanine Hydroxylase (PAH) Protein
Product Overview	This recombinant human Phenylalanine Hydroxylase (PAH) protein includes amino acids 1-226aa of the target gene is expressed in E.coli.The protein is supplied in lyophilized form and formulated in PBSprior to lyophilization.
Target Uniprot Id	P00439
Recommended Name	Phenylalanine-4-hydroxylase
Gene Name	PAH
Synonyms	PKU; PKU1; Phe-4-monooxygenase
Species	Human
Predicted Molecular Mass	28 kDa
Expression System	E.coli
Expression Range	1-226aa
Tag	N-6His
Purity	>90%
Formulation	Lyophilized
Buffer	PBS
Storage Condition	1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C.
Reconstitution Instruction	Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%.
Applications	Positive Control; Immunogen; SDS-PAGE; WB
Research Area	Signal Transduction
Target Function	Catalyzes the hydroxylation of L-phenylalanine to L-tyrosine.
Protein Family	Biopterin-dependent aromatic amino acid hydroxylase family
Associated Diseases	Phenylketonuria (PKU); Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA); Hyperphenylalaninemia (HPA)