目錄:北京索萊寶科技有限公司>>抗體>>Polyclonal Antibody>> K106745PAnti-RDH12 Polyclonal Antibody
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 50ul/100ul |
---|---|---|---|
貨號 | K106745P | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,環(huán)保,化工,生物產(chǎn)業(yè),農(nóng)業(yè) |
主要用途 | WB |
Anti-RDH12 Polyclonal Antibody
英文名稱 | Anti-RDH12 Polyclonal Antibody |
---|---|
宿主 | Rabbit |
別名 | LCA13;LCA3;RDH12;Retinol dehydrogenase 12;SDR7C2;FLJ30273;RP53;SDR7C2 |
應(yīng)用 | WB |
稀釋比例 | WB 1:500-2000. |
交叉反應(yīng) | Human |
蛋白分子量 | 35kDa |
Gene ID | 145226 |
保存 | Store at -20°C. Avoid freeze / thaw cycles. |
儲存液 | Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3. |
純化方法 | Affinity purification |
亞型 | IgG |
免疫原 | Recombinant protein of human RDH12 |
性狀 | 液體 |
Public Immunogen Range | Recombinant protein of human RDH12 |
Subcellular Locations | Cell membrane |
Swiss Prot | Q96NR8 |
克隆類型 | Polyclonal Antibody |
背景資料 | The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53. |