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一(yī)抗

9號染色體開(kāi)放(fàng)閱(yuè)讀(dú)框(kuàng)173抗體(tǐ)

文字:[大(dà)][中(zhōng)][小(xiǎo)] 2017-5-4    瀏覽次數:1743    


英文名(míng)稱(chēng)  Anti-C9orf173  
中文(wén)名稱  9號(hào)染(rǎn)色(sè)體開放閱讀(dú)框(kuàng)173抗(kàng)體(tǐ) 
別    名  C9orf173; Chromosome 9 open reading frame 173; CI173_HUMAN; Uncharacterized protein C9orf173.

詳細(xì)介(jiè)紹(shào):


濃(nóng)    度  1mg/1ml 
規 格(gé)  0.2ml/200μg   
抗體來(lái)源(yuán)  Rabbit  
克(kè)隆(lóng)類型(xíng)  polyclonal 
交叉(chā)反應  Human, Mouse, Rat, Dog   
產品類型  一(yī)抗    
研(yán)究領域  細胞(bāo)生物(wù) 免疫學(xué)  
蛋白分子(zǐ)量  predicted molecular weight: 43kDa 
性    狀  Lyophilized or Liquid 
免 疫 原  KLH conjugated synthetic peptide derived from human C9orf173  
亞(yà)    型  IgG 
純化方(fāng)法  affinity purified by Protein A 
儲(chǔ) 存(cún) 液(yè)  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(shí)蠟切(qiē)片(piàn)需(xū)做抗(kàng)原修(xiū)復(fù)) 
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user.  
保存(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. 

相關資(zī)料:


產(chǎn)品介紹 C9orf173 (chromosome 9 open reading frame 173) is a 389 amino acid protein that exists as four alternatively spliced isoforms. The gene encoding C9orf173 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: Q8N7X2.1


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