HADHSC (HADH) Mouse Monoclonal Antibody [Clone ID: OTI3D12]
CAT#: CF802893
Carrier-free (BSA/glycerol-free) HADH mouse monoclonal antibody, clone OTI3D12 (formerly 3D12)
Formulation: Standard
Frequently bought together (2)
Other products for "HADHSC"
Specifications
| Product Data | |
| Clone Name | OTI3D12 |
| Applications | IHC, WB |
| Recommended Dilution | WB 1:2000, IHC 1:150 |
| Reactivities | Human, Mouse, Rat |
| Host | Mouse |
| Isotype | IgG2a |
| Clonality | Monoclonal |
| Immunogen | Human recombinant protein fragment corresponding to amino acids 57-314 of human HADH (NP_005318) produced in E.coli. |
| Formulation | Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) |
| Reconstitution Method | For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) |
| Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| Conjugation | Unconjugated |
| Storage | Store at -20°C as received. |
| Stability | Stable for 12 months from date of receipt. |
| Predicted Protein Size | 32.8 kDa |
| Gene Name | hydroxyacyl-CoA dehydrogenase |
| Database Link | |
| Background | This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15. [provided by RefSeq, May 2010] |
| Synonyms | HAD; HADH1; HADHSC; HCDH; HHF4; MSCHAD; SCHAD |
| Reference Data | |
| Protein Pathways | Butanoate metabolism, Fatty acid elongation in mitochondria, Fatty acid metabolism, Lysine degradation, Metabolic pathways, Tryptophan metabolism, Valine, leucine and isoleucine degradation |
Documents
| Product Manuals |
| FAQs |
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Resources
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