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產(chǎn)品中心抗體Polyclonal AntibodyK106466PAnti-Occludin Polyclonal Antibody
產(chǎn)品型號(hào)：K106466P
更新時(shí)間：2022-08-15
廠商性質(zhì)：生產(chǎn)廠家
訪 問(wèn) 量 ：1071
010-50973130
產(chǎn)品分類
Anti-Occludin Polyclonal Antibody
| 英文名稱 | Anti-Occludin Polyclonal Antibody |
|---|---|
| 宿主 | Rabbit |
| 別名 | BLCPMG;PPP1R115;BLCPMG;PPP1R115;PTORCH1;OCLN |
| 應(yīng)用 | WB IHC |
| 稀釋比例 | WB 1:2000-5000.IHC 1:50-200. |
| 交叉反應(yīng) | Human Mouse Rat |
| 蛋白分子量 | 53kDa |
| Gene ID | 100506658 |
| 保存 | Store at -20°C. Avoid freeze / thaw cycles. |
| 儲(chǔ)存液 | Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3. |
| 純化方法 | Affinity purification |
| 亞型 | IgG |
| 免疫原 | A synthetic peptide of human Occludin |
| 性狀 | 液體 |
| Public Immunogen Range | A synthetic peptide of human Occludin |
| Subcellular Locations | Cytoplasm |
| Swiss Prot | Q16625 |
| 克隆類型 | Polyclonal Antibody |
| 背景資料 | This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. |
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