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5號染色(sè)體開(kāi)放閱(yuè)讀框(kuàng)35抗(kàng)體

文字(zì):[大(dà)][中][小(xiǎo)] 2017-5-4    瀏覽(lǎn)次數:2509    


英(yīng)文(wén)名(míng)稱  Anti-C5orf35 
中文名稱  5號染(rǎn)色(sè)體開放閱(yuè)讀(dú)框(kuàng)35抗體(tǐ) 
別    名  C5orf35 chromosome 5 open reading frame 35; Chromosome 5 open reading frame 35; Hypothetical protein LOC133383; MGC33648; Uncharacterized protein C5orf35; SET domain-containing protein 9; SETD9_HUMAN. 

詳細介(jiè)紹(shào):


濃(nóng)    度(dù)  1mg/1ml 
規 格  0.2ml/200μg 
抗體來(lái)源(yuán)  Rabbit  
克隆(lóng)類型  polyclonal 
交叉(chā)反(fǎn)應  Human, Dog  
產(chǎn)品(pǐn)類型(xíng)  一抗    
研究領(lǐng)域(yù)  細(xì)胞生(shēng)物(wù) 免(miǎn)疫(yì)學  
蛋白分(fēn)子量(liáng)  predicted molecular weight: 34kDa 
性(xìng)    狀(zhuàng)  Lyophilized or Liquid 
免 疫 原  KLH conjugated synthetic peptide derived from human C5orf35 
亞(yà)    型  IgG 
純化(huà)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(shí)蠟切(qiē)片需做抗原(yuán)修復(fù)) 
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user.  
保存條件  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:


產品介紹(shào) C5orf35 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.
Similarity : Contains 1 SET domain.
Database links : UniProtKB/Swiss-Prot: Q8NE22.2



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