GALE Mouse Monoclonal Antibody [Clone ID: OTI1C4]
CAT#: TA502146M
GALE mouse monoclonal antibody, clone OTI1C4 (formerly 1C4)
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CNY 1350.00
货期*
现货
规格
Specifications
| Product Data | |
| Clone Name | OTI1C4 |
| Applications | IHC, Simple Western, WB |
| Recommend Dilution | WB 1:500~2000, IHC 1:150 ; Simple Western 1:20-1:50 |
| Reactivity | Human, Dog, Rat, Monkey, Mouse |
| Host | Mouse |
| Clonality | Monoclonal |
| Immunogen | Full length human recombinant protein of human GALE (NP_000394) produced in HEK293T cell. |
| Isotype | IgG1 |
| Formulation | PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide. |
| Concentration | 1 mg/ml |
| Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| Conjugation | Unconjugated |
| Storage Condition | Store at -20°C as received. |
| Predicted Protein Size | 38.1 kDa |
| Gene Name | UDP-galactose-4-epimerase |
| Database Link | |
| Background | This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and mental retardation, with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form). Multiple alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Jul 2008] |
| Synonyms | SDR1E1 |
| Reference Data | |
| Protein Families | Druggable Genome |
| Protein Pathways | Amino sugar and nucleotide sugar metabolism, Galactose metabolism, Metabolic pathways |
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