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您当前的位置:首页 > 抗体 > 2号染色体开放阅读框44抗体

2号染色体开放阅读框44抗体

  • 产品货号:mlR9814-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR9814

英文名称 :  C2orf44

中文名称 :  2号染色体开放阅读框44抗体

:  C2orf44; CB044_HUMAN; Chromosome 2 open reading frame 44; FLJ21945; PP384; WD repeat-containing protein C2orf44.  

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, Cow, Sheep,

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 IEM=1:20-200 IGS=1:20-200 GICA=1:20-200 (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.

:  79kDa

细胞定位 :  细胞核 细胞浆

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human C2orf44:251-350/721

    :  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 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. 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 .

PubMed :  PubMed

产品介绍 :   The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrsyndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf44 gene product has been provisionally designated C2orf44 pending further characterization.

Similarity:

Contains 2 WD repeats.

SWISS:

Q9H6R7

Gene ID:

80304

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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