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您当前的位置:首页 > 抗体 > IQCF6蛋白抗体

IQCF6蛋白抗体

  • 产品货号:mlR16691-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品 :  mlR16691

英文名称 :  IQCF6

中文名称 :  IQCF6蛋白抗体

    :  IQ domain-containing protein F6; IQ motif containing F6.  

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,

产品应用 :  WB=1:500-2000 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.

细胞定位 :  细胞浆

    :  Lyophilized or Liquid

    :  1mg/ml

 :  KLH conjugated synthetic peptide derived from human IQCF6:1-100/107

    :  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background:

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

Function:

May play a regulatory role in spermatogenesis.

Tissue Specificity:

Expressed in fetal and adult testis, in germ cells but not somatic cells.

Similarity:

Contains 1 IQ domain.

SWISS:

Q86VS3

Gene ID:

64799

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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