| 英文名稱 | Rabbit MYH9 Polyclonal Antibody |
|---|
| 別名 | BDPLT6;DFNA17;EPSTS;FTNS;MHA;NMHC-II-A;NMMHC-IIA;NMMHCA
|
|---|
| 應(yīng)用 | WB,IHC |
|---|
| 稀釋比例 | WB1:1000-1:2000 IHC1:50-1:100 |
|---|
| 交叉反應(yīng) | Human Mouse |
|---|
| 蛋白分子量 | 227kDa |
|---|
| Gene ID | 4627 |
|---|
| 保存 | Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment. |
|---|
| 儲存液 | PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
|---|
| 純化方法 | Affinity purification |
|---|
| 亞型 | IgG |
|---|
| 免疫原 | Recombinant protein of human MYH9 |
|---|
| 性狀 | Lyophilized or Liquid |
|---|
| Swiss Prot | P35579 |
|---|
| 克隆類型 | Polyclonal Antibody |
|---|
| 來源 | Rabbit |
|---|
| 背景資料 | This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.
|
|---|
