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货号： bs-14391R-Cy5 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-14391R-Cy5
- 英文名称
- Anti-DNAJC30/Cy5
- 中文名称
- Cy5标记的DNAJC30蛋白抗体
- 别 名
- DnaJ (Hsp40) homolog subfamily C member 30; DnaJ homolog subfamily C member 30; DNAJC 30; MGC12943; WBSCR 18; DJC30_HUMAN; WBSCR18; Williams Beuren syndrome chromosomal region 18 protein; Williams Beuren syndrome chromosome region 18.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 细胞生物 信号转导 转运蛋白
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Pig, Rabbit,
- 产品应用
- ICC=1:50-200 IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 25kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human DNAJC30
- 亚 型
- IgG
- 纯化方法
- affinity purified by Protein A
- 储 存 液
- 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
- 保存条件
- Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
- 产品介绍
- background:
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]
Function:
DNAJC30 is 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.
Tissue Specificity:
Expressed in brain, heart, kidney, liver, lung, spleen, stomach and testis.
DISEASE:
Note=DNAJC30 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region.
Similarity:
Contains 1 J domain.
Database links:Entrez Gene: 84277Human
GenBank: BC005056Human
SwissProt: Q96LL9Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.