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您当前的位置:首页 > 抗体 > FAM135B蛋白抗体

FAM135B蛋白抗体

  • 产品货号:mlR9063-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR9063

英文名称 :  FAM135B

中文名称 :  FAM135B蛋白抗体

  :  C8ORFK32; F135B_HUMAN; fam135b; Family with sequence similarity 135 member B; Hypothetical protein LOC51059; MGC126009; MGC126010; MGC33221; Protein FAM135B.  

研究领域 :  肿瘤  细胞生物  免疫学  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应 :   Human, Mouse, Rat,

产品应用 :  WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:50-200 (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.

:  156kDa

细胞定位 :  细胞核 细胞浆 细胞膜

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human FAM135B:1051-1250/1406

    :  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 :   Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM135B gene product has been provisionally designated FAM135B pending further characterization.

Similarity:

Belongs to the FAM135 family.

SWISS:

Q49AJ0

Gene ID:

51059

Important Note:

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

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