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您当前的位置:首页 > 抗体 > 7号染色体开放阅读框39抗体

7号染色体开放阅读框39抗体

  • 产品货号:mlR18531-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR18531

英文名称 :  ZC3HAV1L/C7orf39

中文名称 :  7号染色体开放阅读框39抗体

  :  B130055L09Rik; C7orf39; E430016P22Rik; RGD1309236; Zc3hav1l; ZCCHL_HUMAN; Zinc finger CCCH-type antiviral protein 1-like.  

研究领域 :  神经生物学  细胞膜受体  表观遗传学  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应 :   Human,

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.

:  33kDa

细胞定位 :  细胞浆

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human ZC3HAV1L/C7orf39:201-300/300

    :  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 :   ZC3HAV1L is a 296 amino acid protein that contains two C3H1-type zinc fingers. Existing as two alternatively spliced isoforms, the gene encoding ZC3HAV1L maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

Post-translational modifications:

Phosphorylated upon DNA damage, probably by ATM or ATR.

SWISS:

Q96H79

Gene ID:

92092

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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