Phenylalanine Hydroxylase antibody (AA 1-290)

Catalog No. ABIN3015513

Product Details anti-Phenylalanine Hydroxylase Antibody

Target: Phenylalanine Hydroxylase

Binding Specificity: AA 1-290

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Phenylalanine Hydroxylase antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Sequence: MSTAVLENPG LGRKLSDFGQ ETSYIEDNCN QNGAISLIFS LKEEVGALAK VLRLFEENDV NLTHIESRPS RLKKDEYEFF THLDKRSLPA LTNIIKILRH DIGATVHELS RDKKKDTVPW FPRTIQELDR FANQILSYGA ELDADHPGFK DPVYRARRKQ FADIAYNYRH GQPIPRVEYM EEEKKTWGTV FKTLKSLYKT HACYEYNHIF PLLEKYCGFH EDNIPQLEDV SQFLQTCTGF RLRPVAGLLS SRDFLGGLAF RVFHCTQYIR HGSKPMYTPE PDICHELLGH

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-290 of human PAH (NP_000268.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:200

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Phenylalanine Hydroxylase

Target: Phenylalanine Hydroxylase

Alternative Name: PAH (Phenylalanine Hydroxylase Products)

Synonyms: cb877 antibody, wu:fb02f10 antibody, zgc:65981 antibody, GB18494 antibody, PAH antibody, pku antibody, pku1 antibody, DDBDRAFT_0206188 antibody, DDBDRAFT_0231664 antibody, DDB_0206188 antibody, DDB_0231664 antibody, AW106920 antibody, PH antibody, PKU antibody, PKU1 antibody, phenylalanine-4-hydroxylase antibody, phenylalanine hydroxylase antibody, protein henna antibody, phenylalanine 4-monooxygenase antibody, pah antibody, LOC408622 antibody, PAH antibody, CpipJ_CPIJ002149 antibody, Pah antibody

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.,PAH,PH,PKU,PKU1,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,PAH

Molecular Weight: 51 kDa

Gene ID: 5053

UniProt: P00439