DNAJC30 抗体
(DnaJ (Hsp40) Homolog, Subfamily C, Member 30 (DNAJC30))
This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene 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 |
|---|---|---|---|---|---|
| DNAJC30 抗体 (Center) | 人, 小鼠 | 兔 Polyclonal |
|
|
Primary Antibody
- WB (Western Blotting: 所列应用)
- 适用
- 人, 小鼠
- 宿主
- 兔
- 克隆形成能力
- Polyclonal
- 标记
- unconjugated
- 抗原表位
- Center
Latest Publications for our DNAJC30 抗体
: "The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development. ..." in: Cell, Vol. 175, Issue 4, pp. 1088-1104.e23, (2018) (PubMed).
Aliases for DNAJC30 抗体
DnaJ heat shock protein family (Hsp40) member C30 (DNAJC30) 抗体DnaJ heat shock protein family (Hsp40) member C30 (Dnajc30) 抗体
1300007M11Rik 抗体
WBSCR18 抗体
Wbscr18 抗体
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