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一(yī)抗(kàng)

9號染色體開放閱(yuè)讀(dú)框139抗體(tǐ)

文字(zì):[大][中][小] 2017-5-4    瀏覽次數(shù):1634    


英文名(míng)稱(chēng)  Anti-C9orf139 
中(zhōng)文名(míng)稱  9號染(rǎn)色體開(kāi)放閱(yuè)讀框(kuàng)139抗(kàng)體 
別(bié)    名(míng)  C9orf139; Chromosome 9 open reading frame 139; CI139_HUMAN; Uncharacterized protein C9orf139.

詳(xiáng)細(xì)介紹:


濃(nóng)    度  1mg/1ml 
規 格(gé)  0.2ml/200μg
抗(kàng)體來(lái)源  Rabbit  
克隆類型(xíng)  polyclonal 
交(jiāo)叉(chā)反應  Human   
產(chǎn)品(pǐn)類型(xíng)  一(yī)抗    
研(yán)究(jiū)領(lǐng)域  細胞(bāo)生物(wù) 免疫學  
蛋(dàn)白(bái)分子(zǐ)量  predicted molecular weight: 20kDa 
性    狀  Lyophilized or Liquid 
免(miǎn) 疫 原(yuán)  KLH conjugated synthetic peptide derived from human C9orf139 
亞(yà)    型  IgG 
純化方法(fǎ)  affinity purified by Protein A 
儲(chǔ) 存(cún) 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4 
產(chǎn)品應(yīng)用   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(shí)蠟切(qiē)片(piàn)需(xū)做(zuò)抗原(yuán)修復(fù)) 
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user.  
保(bǎo)存(cún)條件  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. 
Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

相(xiāng)關(guān)資料:


產品(pǐn)介紹 C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Database links : UniProtKB/Swiss-Prot: Q6ZV77.1



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