Rabbit Anti-DNAJC30/FITC Conjugated antibody
|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|
|交叉反应||Human, Mouse, Rat, Pig, Rabbit,|
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|
|免 疫 原||KLH conjugated synthetic peptide derived from human DNAJC30|
|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.|
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]
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.
Expressed in brain, heart, kidney, liver, lung, spleen, stomach and testis.
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.
Contains 1 J domain.
Entrez Gene: 84277 Human
GenBank: BC005056 Human
SwissProt: Q96LL9 Human
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications
该无内含子基因编码DNJ分子伴侣同源结构域包含蛋白家族的成员。该基因在Williams综合征中缺失，Williams综合征是一种多系统发育障碍，由7q11.23处的相邻基因缺失引起。[ RefSeq，JUL 2008 ]