目錄:北京索萊寶科技有限公司>>抗體>>Polyclonal Antibody>> K106550PAnti-Desmin Polyclonal Antibody
| 供貨周期 | 現貨 | 規格 | 50ul /100ul |
|---|---|---|---|
| 貨號 | K106550P | 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 |
Anti-Desmin Polyclonal Antibody
| 英文名稱 | Anti-Desmin Polyclonal Antibody |
|---|---|
| 宿主 | Rabbit |
| 別名 | CSM1;CSM2;LGMD2R;DES;Desmin |
| 應用 | WB |
| 稀釋比例 | WB 1:3000. |
| 交叉反應 | Human Mouse Rat |
| 蛋白分子量 | 65kDa |
| Gene ID | 1674 |
| 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 Desmin |
| 性狀 | 液體 |
| Public Immunogen Range | A synthetic peptide of human Desmin |
| Subcellular Locations | Cell membrane Cytoplasm sarcolemma |
| Swiss Prot | P17661 |
| 克隆類型 | Polyclonal Antibody |
| 背景資料 | Defects in Desmin are the cause of desmin related cardio skeletal myopathy (CSM) also known as desmin related myopathy (DRM). CSM is characterized by skeletal muscle weakness associated with cardiac conduction blocks, arrhythmias, restrictive heart failure, and by intracytoplasmic accumulation of desmin reactive deposits in cardiac and skeletal muscle cells. A desmin related myopathy can have a distal onset, it is then known as hereditary distal myopathy (HDM). Defects in Desmin are also the cause of dilated cardiomyopathy type 1I (CMD1I). CMD1I is an autosomal form of dilated cardiomyopathy characterized by ventricular dilatation and impaired systolic function. |
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