HAL antibody
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- Target See all HAL Antibodies
- HAL (Histidine Ammonia-Lyase (HAL))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This HAL antibody is un-conjugated
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by peptide affinity chromatography method.
- Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human HAL.
- Top Product
- Discover our top product HAL Primary Antibody
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- Application Notes
- 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
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- 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.
- 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.
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- 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 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.
- Molecular Weight
- 72 kDa
- Gene ID
- 3034
- NCBI Accession
- NP_002099
- UniProt
- P42357
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