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Beta-Glycerophosphate, Disodium Sal
zymet BGA底部密封剂1412
【正品直销，售后保障】（small RNA文
通过抚州高新技术产业开发区市场和质量监督管理局认证 
| 货号： | K005495P |
| 供应商： | 江蓝纯 |
| 数量： | 99 |
| 规格： | 50ul/100ul |
| 英文名称 | Rabbit TBL1XR1 Polyclonal Antibody |
|---|---|
| 应用 | WB,IHC,IF |
| 稀释比例 | WB1:500-1:2000 IHC1:50-1:200 IF1:50-1:100 |
| 交叉反应 | Human,Mouse,Rat |
| 蛋白分子量 | 56kDa |
| Gene ID | 79718 |
| 保存 | Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment. |
| 储存液 | PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| 纯化方法 | Affinity purification |
| 亚型 | IgG |
| 免疫原 | Recombinant protein of human TBL1XR1 |
| 性状 | Lyophilized or Liquid |
| Swiss Prot | Q9BZK7 |
| 克隆类型 | Polyclonal Antibody |
| 来源 | Rabbit |
| 背景资料 | This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. |
温馨提示：不可用于临床治疗。
