| 產(chǎn)品編號 | bs-42206P |
| 英文名稱 | Recombinant mouse FOXN1 protein, N-GST |
| 中文名稱 | 重組小鼠叉頭蛋白N1 |
| 別 名 | FKHL20; Forkhead box N1; Forkhead box protein N1; FOXN 1; FOXN1_HUMAN; FOXN1_MOUSE;RONU; Rowett nude; Transcription factor winged-helix nude; WHN; Winged helix nude; Winged-helix transcription factor nude. |
| 理論分子量 | 44.4kDa |
| 性 狀 | Liquid |
| 濃 度 | >1mg/ml |
| 物 種 | Mouse |
| 序 列 | 8-172/648 |
| 純 度 | >90% as determined by SDS-PAGE |
| 純化方法 | AC |
| 內(nèi)毒素 | Not analyzed |
| 表達(dá)系統(tǒng) | E.coli |
| 標(biāo)簽 | N-GST |
| 緩 沖 液 | PBS (pH=7.4) with 15mM GSH and .5mM PMSF |
| 保存條件 | Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles. |
| 注意事項 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 產(chǎn)品介紹 | Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008]. SWISS: O15353 Gene ID: 8456 |
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