HAL antibody

Catalog No. ABIN2462882

Product Details anti-HAL Antibody

Target: HAL (Histidine Ammonia-Lyase (HAL))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HAL antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Purification: Antibody is purified by protein A chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human HAL.

Application Details

Application Notes: HAL antibody can be used for detection of HAL by ELISA at 1:312500. HAL antibody can be used for detection of HAL by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store HAL antibody at -20 °C.

Target Details for HAL

Target: HAL (Histidine Ammonia-Lyase (HAL))

Alternative Name: HAL (HAL Products)

Synonyms: HIS antibody, HSTD antibody, hal antibody, hstd antibody, xhal antibody, HAL antibody, BA3712 antibody, DDBDRAFT_0187742 antibody, DDBDRAFT_0231727 antibody, DDB_0187742 antibody, DDB_0231727 antibody, zgc:136980 antibody, his antibody, Hsd antibody, histidase antibody, histidine ammonia-lyase antibody, histidine ammonia-lyase, gene 1 L homeolog antibody, histidine ammonia-lyase HutH antibody, histidine ammonia-lyase, gene 1 antibody, histidine ammonia lyase antibody, HAL antibody, hal.1.L antibody, hutH antibody, Tc00.1047053506247.220 antibody, Plav_1493 antibody, hal antibody, hal.1 antibody, Hal antibody

Background: HAL is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. HAL defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluidsHistidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids.

Molecular Weight: 72 kDa

Gene ID: 3034

NCBI Accession: NP_002099

UniProt: P42357