RDH5 抗体
-
- 抗原 See all RDH5 抗体
- RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This RDH5 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human RDH5. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product RDH5 Primary Antibody
-
-
- 应用备注
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
-
Positive Control: NT2D1
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
-
- 抗原
- RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
- 别名
- retinol dehydrogenase 5 (RDH5 产品)
- 别名
- 9cRDH antibody, HSD17B9 antibody, RDH1 antibody, SDR9C5 antibody, RDHB antibody, MGC84134 antibody, RDH5 antibody, rdh1 antibody, hsd17b9 antibody, im:6901729 antibody, si:dkey-102c8.5 antibody, 9-cis antibody, AI987873 antibody, RDH4 antibody, cRDH antibody, retinol dehydrogenase 5 antibody, retinol dehydrogenase 1 antibody, retinol dehydrogenase 5 L homeolog antibody, retinol dehydrogenase 5 (11-cis/9-cis) antibody, RDH5 antibody, rdh1 antibody, rdh5.L antibody, rdh5 antibody, Rdh5 antibody
- 背景
- Retinol dehydrogenase 5 , 9cRDH , HSD17B9 , RDH1 , SDR9C5,This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. [provided by RefSeq]
- 分子量
- 35 kDa
- 基因ID
- 5959
- UniProt
- Q92781
-