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您当前的位置:首页 > 抗体 > 肺腺瘤易感蛋白2抗体

肺腺瘤易感蛋白2抗体

  • 产品货号:mlR9672-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR9672

英文名称 :  LAS2

中文名称 :  肺腺瘤易感蛋白2抗体

  :  Chromosome 18 open reading frame 54; Hypothetical protein LOC162681; LAS2; Lung adenoma susceptibility protein 2; MGC33382; Uncharacterized protein C18orf54; LAS2_HUMAN.  

研究领域 :  心血管  细胞生物  免疫学  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应 :   Human, Mouse, Rat, Pig,

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.

:  39/60kDa

细胞定位 :  分泌型蛋白

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human LAS2/C18orf54:301-372/372

    :  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 :   Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.

Function:

Might play a role in cell proliferation.

Subcellular Location:

Secreted.

SWISS:

Q8IYD9

Gene ID:

162681

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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