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今(jīn)天是2026年7月(yuè)22日 星(xīng)期三,歡迎(yíng)光(guāng)臨本(běn)站 上海研生(shēng)實業有限(xiàn)公(gōng)司 網址: darylliu.cn

一抗

7號染(rǎn)色(sè)體開放閱讀(dú)框43抗(kàng)體

文字(zì):[大][中(zhōng)][小(xiǎo)] 2017-5-4    瀏覽次(cì)數:2351    


英文名(míng)稱  Anti-C7orf 43 
中(zhōng)文名稱  7號(hào)染(rǎn)色(sè)體開放閱讀框(kuàng)43抗體(tǐ) 
別    名(míng)  Uncharacterized protein C7orf43; CG043_HUMAN; C7orf43; Chromosome 7 open reading frame 43; DKFZp761G0712; FLJ10925; Hypothetical protein LOC55262.  

詳(xiáng)細介紹:


濃(nóng)    度  1mg/1ml 
規 格  0.2ml/200μg  
抗體(tǐ)來源(yuán)  Rabbit  
克隆類(lèi)型  polyclonal 
交叉反(fǎn)應(yīng)  Human, Mouse, Rat, Dog, Pig, Cow, Rabbit, Sheep   
產品類型  一抗    
研究(jiū)領(lǐng)域  細胞(bāo)生(shēng)物 免疫學  
蛋白分子(zǐ)量  predicted molecular weight: 62kDa 
性    狀  Lyophilized or Liquid 
免 疫(yì) 原  KLH conjugated synthetic peptide derived from human C7ORF43 
亞    型(xíng)  IgG 
純(chún)化方法(fǎ)  affinity purified by Protein A 
儲 存 液(yè)  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4 
產品(pǐn)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(là)切(qiē)片(piàn)需做(zuò)抗原修復) 
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user.  
保存(cún)條(tiáo)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. 

相關(guān)資料(liào):


產品(pǐn)介紹(shào) Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. 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 C7orf43 gene product has been provisionally designated C7orf43 pending further characterization.
Database links : UniProtKB/Swiss-Prot: Q8WVR3.2



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