目錄:北京索萊寶科技有限公司>>抗體>>Polyclonal Antibody>> K106466PAnti-Occludin Polyclonal Antibody
| 供貨周期 | 現貨 | 規格 | 50ul/100ul |
|---|---|---|---|
| 貨號 | K106466P | 應用領域 | 醫療衛生,環保,化工,生物產業,農林牧漁 |
| 主要用途 | WB IHC |
Anti-Occludin Polyclonal Antibody
| 英文名稱 | Anti-Occludin Polyclonal Antibody |
|---|---|
| 宿主 | Rabbit |
| 別名 | BLCPMG;PPP1R115;BLCPMG;PPP1R115;PTORCH1;OCLN |
| 應用 | WB IHC |
| 稀釋比例 | WB 1:2000-5000.IHC 1:50-200. |
| 交叉反應 | Human Mouse Rat |
| 蛋白分子量 | 53kDa |
| Gene ID | 100506658 |
| 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 | 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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