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您当前的位置:首页 > 抗体 > 21号染色体开放阅读框25抗体

21号染色体开放阅读框25抗体

  • 产品货号:mlR9988-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR9988

英文名称 :  C21orf25

中文名称 :  21号染色体开放阅读框25抗体

   :  C2 calcium-dependent domain containing 2; C2 domain containing protein 2; C21orf25; C21orf258; C2CD2; Chromosome 21 open reading frame 25; MGC71445; TMEM24-like; TMEM24L; CU025_HUMAN.  

研究领域 :  细胞生物  发育生物学  神经生物学  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应 :   Human, Mouse, Rat, Pig, Cow, Horse, Rabbit, Sheep,

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.

:  71kDa

细胞定位 :  分泌型蛋白

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human C2CD2/C21orf25:451-550/696

    :  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 :   The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C2CD2 is an 696 amino acid protien that is secreted. The C2CD2 gene product has been provisionally designated C2CD2 pending further characterization.

Subcellular Location:

Secreted.

Similarity:

Contains 1 C2 domain.

SWISS:

Q9Y426

Gene ID:

25966

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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