产品货号：
Z10652
中文名称：
ALDH3A2抗体
英文名称：
Anti-ALDH3A2 Antibody
产品规格：
0.1mg
发货周期：
1～3天
产品价格：
询价
| 抗体名称 | Anti-ALDH3A2 Antibody |
| 指标别名 | Aldehyde dehydrogenase 10;ALDH10;ALDH3A2;FALDH;Fatty aldehyde dehydrogenase;SLS |
| 克隆性 | Polyclonal |
| 检验物种 | human,mouse |
| 应用范围 | ELISA,WB |
| 基因名称 | ALDH3A2 |
| 抗体来源 | Rabbit |
| 抗体类型 | IgG |
| 免疫原 | Aldh3A2 antibody was raised against a 14 amino acid synthetic peptide near the carboxy terminus of the human Aldh3A2.The immunogen is located within the last 50 amino acids of Aldh3A2. |
| 计算分子量 | 55kDa |
| 成分 | Aldh3A2 Antibody is supplied in PBS containing 0.02% sodium azide. |
| 纯化方式 | Aldh3A2 Antibody is affinity chromatography purified via peptide column. |
| 浓度 | 1mg/mL |
| 产品形态 | 溶液 |
| 保存条件 | 4℃可保存3个月，-20℃可保存1年。 |
| 背景资料 | Aldh3A2 is a member of the aldehyde dehydrogenase superfamily,a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes.Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation.Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids.Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome,an inherited neurocutaneous disorder.Patients with this disorder display ichthyosis,mental retardation and spastic diplegia.The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain,the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins,or defective eicosanoid metabolism. |
| Uniprot ID | P51648 |
| 基因名全称 | Aldehyde dehydrogenase 3 family,member A2 |
| 蛋白名全称 | Aldehyde dehydrogenase 3 family,member A2 |
| 推荐稀释比 | Aldh3A2 antibody can be used for detection of Aldh3A2 by Western blot at 1 ～ 2μg/mL.Antibody validated:Western Blot in mouse samples.All other applications and species not yet tested. |
相关搜索：ALDH3A2抗体，ALDH3A2多抗，Anti-ALDH3A2 Antibody