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5号染色体开放阅读框36抗体

  • 产品货号:mlR18918-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品 :  mlR18918

英文名称 :  C5orf36

中文名称 :  5号染色体开放阅读框36抗体

    :  MGC34713; C5orf36; Chromosome 5 open reading frame 36; Hypothetical protein LOC285600; K0825_HUMAN; KIAA0825; Uncharacterized protein KIAA0825.  

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 :  Human, Mouse, Rat, Chicken, Dog, Cow, Horse, Rabbit, Sheep,

产品应用 :  ELISA=1:500-1000 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.

:  148kDa

细胞定位 :  细胞核 细胞浆 细胞外基质

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human C5orf36:551-650/1275

    :  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 :  With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf36 gene product has been provisionally designated C5orf36 pending further characterization.

SWISS:

O94914

Gene ID:

285600

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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