投诉建议和代测服务及先货发票情况:13818158258 |

老网站

微信公众号二维码

关注微信公众号

手机站二维码

前往手机站

邮件订阅产品说明书或动态
您当前的位置:首页 > 抗体 > 10号染色体开放阅读框96抗体

10号染色体开放阅读框96抗体

  • 产品货号:mlR24138-1 收藏此商品
  • 销售价:880.00-2480.00
规格:
50ul 100ul 200ul
购买数量:
+
立即购买
加入购物车

免费咨询电话:021-54222852 / 15216759556

【友情提示】:产品价格与说明书请点击上面的链接,在线询价,索要说明书

产品 :  mlR24138

英文名称 :  C10orf96

中文名称 :  10号染色体开放阅读框96抗体

    :  MGC35062 C10orf96; CCDC172; chromosome 10 open reading frame 96; hypothetical protein LOC374355; UPF0628 protein C10orf96.  

研究领域 :  细胞生物  免疫学  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应  :  Mouse, Rat,

产品应用 :  IHC-P=1:400-800 IHC-F=1:400-800 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

:  31kDa

细胞定位 :  细胞浆 细胞膜

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from mouse C10orf96 :61-160/267

    :  IgG

纯化方法 :  affinity purified by Protein A

:  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.

PubMed :  PubMed

产品介绍 :   C10orf96 is a 258 amino acid protein belonging to the UPF0628 family and is encoded by a gene located on human chromosome 10. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolmans syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

SWISS:

Q810N9

Gene ID:

75645

Important Note:

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

产品图片


购买人 出价 数量 购买时间 状态
我要咨询
发表话题
讨论内容:
验证码:
  • 公司资讯
  • 产品文献