产品货号：
Z37667
中文名称：
GALE抗体
英文名称：
Anti-GALE Antibody (Clone#OTI1C4)
产品规格：
50μl|100μl|150μl
发货周期：
1～3天
产品价格：
询价
| 抗体名称 | Anti-GALE Antibody (Clone#OTI1C4) |
| 指标别名 | Galactowaldenase;GALE;SDR1E1;UDP glucose 4 epimerase;UDP-galactose-4-epimerase |
| 克隆性 | Monoclonal |
| 检验物种 | human,monkey,mouse,rat,dog |
| 应用范围 | WB,IHC |
| 基因名称 | GALE |
| 克隆号 | OTI1C4 |
| 抗体来源 | Mouse |
| 抗体类型 | IgG1 |
| 免疫原 | Full length human recombinant protein of human GALE (NP_000394) produced in HEK293T cell. |
| 实际分子量 | 38.1KD |
| 成分 | PBS (PH 7.3) containing 1% BSA,50% glycerol and 0.02% sodium azide. |
| 纯化方式 | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| 浓度 | 500μg/mL |
| 产品形态 | 溶液 |
| 保存条件 | Stable for 12 months from date of receipt.Store at -20℃ as received. |
| 背景资料 | 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] |
| Uniprot ID | Q14376 |
| 基因名全称 | UDP-galactose-4-epimerase |
| 蛋白名全称 | UDP-glucose 4-epimerase |
| 推荐稀释比 | Western blot (WB) 1:500～2000 Immunohistochemistry in paraffin section (IHC) 1:150 |
相关搜索：GALE抗体，GALE单抗，Anti-GALE Antibody (Clone#OTI1C4)