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今天(tiān)是2026年7月21日(rì) 星(xīng)期二(èr),歡迎(yíng)光臨本站(zhàn) 上海研生實業有限(xiàn)公(gōng)司 網址: darylliu.cn

一抗

9號(hào)染(rǎn)色(sè)體開放閱(yuè)讀框(kuàng)79抗(kàng)體

文字:[大][中(zhōng)][小] 2017-5-4    瀏覽(lǎn)次(cì)數:1577    


英(yīng)文名稱  Anti-C9orf79  
中(zhōng)文(wén)名(míng)稱  9號染色(sè)體(tǐ)開放閱(yuè)讀框79抗(kàng)體 
別(bié)    名  C9orf79; Chromosome 9 open reading frame 79; S31E1_HUMAN; FAM75-like protein C9orf79. 

詳(xiáng)細介紹:


濃    度  1mg/1ml 
規 格(gé)  0.2ml/200μg    
抗(kàng)體來源(yuán)  Rabbit  
克隆(lóng)類型  polyclonal 
交叉反(fǎn)應(yīng)  Human   
產(chǎn)品(pǐn)類(lèi)型(xíng)  一抗    
研究(jiū)領域(yù)  細胞(bāo)生(shēng)物(wù) 免疫學  
蛋白分子量  predicted molecular weight: 157kDa 
性    狀  Lyophilized or Liquid 
免(miǎn) 疫(yì) 原  KLH conjugated synthetic peptide derived from human C9orf79  
亞    型(xíng)  IgG 
純(chún)化(huà)方(fāng)法(fǎ)  affinity purified by Protein A 
儲 存 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4 
產品應用   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 
(石蠟(là)切片需(xū)做(zuò)抗原修復(fù)) 
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user.  
保(bǎo)存(cún)條件(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(guān)資料(liào):


產品(pǐn)介紹 C9orf79 is a 1,445 amino acid single-pass membrane protein that belongs to the FAM75 family. The gene encoding C9orf79 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered 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.
Function : May play a role in spermatogenesis (By similarity).
Subcellular Location : Membrane; Single-pass membrane protein (Potential).
Similarity : Belongs to the SPATA31 family.
Database links : UniProtKB/Swiss-Prot: Q6ZUB1.2





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