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今天(tiān)是2026年7月23日 星(xīng)期四(sì),歡迎光臨本站(zhàn) 上海研(yán)生實(shí)業有(yǒu)限(xiàn)公司 網址: darylliu.cn

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FITC標記(jì)的腺(xiàn)瘤樣(yàng)息肉(ròu)抗(kàng)體(tǐ)

文(wén)字(zì):[大][中][小] 2017-5-3    瀏(liú)覽次數(shù):1610    

                                   FITC標(biāo)記的腺瘤樣息(xī)肉抗體(tǐ)                                                                                                                                                
英(yīng)文名稱Anti-APC/FITC
中(zhōng)文名稱:FITC標(biāo)記(jì)的(dí)腺(xiàn)瘤(liú)樣(yàng)息肉(ròu)抗體
別    名Adenomatous Polyposis Coli; Adenomatous polyposis coli protein; APC_HUMAN; CC1; Deleted in polyposis 2.5; DP2; DP2.5; DP3; FAP; FPC; GS; Protein APC.  

詳(xiáng)細(xì)介(jiè)紹(shào):


規格:100ul 
說(shuō) 明(míng) 書100ul  
研(yán)究(jiū)領域腫瘤(liú)  心(xīn)血管(guǎn)  細胞生(shēng)物  免疫學  發(fā)育(yù)生物學(xué)  染(rǎn)色質和核信號  神經(jīng)生(shēng)物學  信(xìn)號(hào)轉導  幹(gān)細(xì)胞  細胞(bāo)周期(qī)蛋白  轉錄調(tiáo)節因子(zǐ)  腫瘤(liú)細(xì)胞(bāo)生(shēng)物標誌(zhì)物(wù)  表觀(guān)遺傳(chuán)學(xué)  
抗體來源(yuán)Rabbit
克隆(lóng)類型(xíng)Polyclonal
交叉(chā)反應(yīng) Human, Mouse, Rat, Pig, Cow, Horse, Rabbit, 
產品應用(yòng)IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分(fēn) 子(zǐ) 量312kDa
細胞(bāo)定(dìng)位(wèi)細胞膜 
性    狀(zhuàng)Lyophilized or Liquid
濃    度(dù)1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human APC
亞(yà)    型IgG
純(chún)化方法affinity purified by Protein A
儲(chǔ) 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存(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.

相關資(zī)料(liào):


產品(pǐn)介紹background:
This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq]

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