HAL anticorps

N° du produit ABIN2458951

Détail du produit anti-HAL anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HAL est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

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

Information d'application

Indications d'application: HAL antibody can be used for detection of HAL by ELISA at 1:1562500. HAL antibody can be used for detection of HAL by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?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.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

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

Détails sur HAL

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

Autre désignation: HAL (HAL Produits)

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

Sujet: 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 fluids Histidine 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.

Poids moléculaire: 72 kDa

ID gène: 3034

NCBI Accession: NP_002099

UniProt: P42357