WBSCR16 抗体
(Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))
This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008].
| Catalog no. | 产品 | 适用 | 宿主 / 克隆类型 | 应用 | 价格和交货时间 |
|---|---|---|---|---|---|
| WBSCR16 抗体 (Alexa Fluor 594) | 人, 小鼠 | 兔 Polyclonal |
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| WBSCR16 抗体 (Alexa Fluor 488) | 人, 小鼠 | 兔 Polyclonal |
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| WBSCR16 抗体 | 人, 小鼠, 大鼠 | 兔 Polyclonal |
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Primary Antibody
- WB (Western Blotting: 所列应用)
- IF (Immunofluorescence: 所列应用)
- 适用
- 人, 小鼠, 大鼠
- 宿主
- 兔
- 克隆形成能力
- Polyclonal
- 标记
- unconjugated
Aliases for WBSCR16 抗体
RCC1 like (RCC1L) 抗体reculator of chromosome condensation 1 like (Rcc1l) 抗体
5730496C04Rik 抗体
AU019812 抗体
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