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7號(hào)染(rǎn)色體開放(fàng)閱(yuè)讀框53抗體(tǐ)

文(wén)字(zì):[大(dà)][中][小] 2017-5-4    瀏覽(lǎn)次數(shù):1714    


英文名稱(chēng)  Anti-C7orf53 
中文(wén)名(míng)稱  7號染色體開放閱讀框(kuàng)53抗體(tǐ) 
別    名  C7orf53; CG053_HUMAN; Chromosome 7 open reading frame 53; Coiled-coil domain-containing transmembrane protein C7orf53. 

詳細介(jiè)紹:


濃(nóng)    度  1mg/1ml 
規 格  0.2ml/200μg   
抗(kàng)體來(lái)源  Rabbit  
克隆(lóng)類(lèi)型  polyclonal 
交(jiāo)叉(chā)反應(yīng)  Human, Mouse, Rat, Dog  
產品類(lèi)型(xíng)  一抗(kàng)    
研(yán)究(jiū)領(lǐng)域(yù)  細(xì)胞生(shēng)物(wù) 免(miǎn)疫學  
蛋白(bái)分子量(liáng)  predicted molecular weight: 14kDa 
性    狀  Lyophilized or Liquid 
免(miǎn) 疫(yì) 原  KLH conjugated synthetic peptide derived from human C7orf53 
亞(yà)    型(xíng)  IgG 
純(chún)化(huà)方(fāng)法  affinity purified by Protein A 
儲 存(cún) 液(yè)  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4 
產品應(yīng)用(yòng)   WB=1:100-500  ELISA=1:500-1000  IP=1:20-100  IHC-P=1:100-500  IHC-F=1:100-500  ICC=1:100-500  IF=1:100-500 
(石蠟(là)切片需做抗原修(xiū)復(fù)) 
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user.  
保存條件(jiàn)  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. 
Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

相(xiāng)關資料:


產品(pǐn)介紹 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. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterization.
Subcellular Location : Membrane; Single-pass membrane protein (Potential). 
Database links : UniProtKB/Swiss-Prot: Q8N8F7.1



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