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基因克隆與定點突變服務(wù)|實驗技術(shù)服務(wù)

時間:2015/7/1閱讀:267
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關(guān)鍵詞:基因克隆與定點突變服務(wù)|實驗技術(shù)服務(wù)
簡介:世界*品牌基因克隆與定點突變服務(wù)|實驗技術(shù)服務(wù)原裝,,質(zhì)量保證,*,。
基因克隆與定點突變服務(wù)|實驗技術(shù)服務(wù)——pCzn1質(zhì)粒+Arctic Express宿主菌低溫表達體系。
我們具備豐富的蛋白表達設(shè)計經(jīng)驗及實驗操作技巧,,承諾客戶不成功不收費,。我們所有的實驗數(shù)據(jù)真實可信,我們提供原始的表達菌株和克隆質(zhì)粒,,客戶可以依據(jù)我們的實驗報告重復(fù)我們的實驗結(jié)果,。
產(chǎn)品品牌:   http://www.。,。com/goodsid/fenleiyi/2868603/1.html    
測序?qū)嶒灹鞒蹋?br>定點突變是指通過聚合酶鏈式反應(yīng)(PCR)等方法向目的DNA段(可以是基因組,,也可以是質(zhì)粒)中引入所需變化(通常是表征有利方向的變化),包括堿基的添加,、刪除,、點突變等。定點突變能迅速,、的提高DNA所表達的目的蛋白的性狀及表征,,是基因研究工作中一種非常有用的手段,。
定點突變的比較有特色的產(chǎn)品還有Clontech公司的Transformer Site-Directed Mutagenesis Kit,需要根據(jù)準備突變的質(zhì)粒自行設(shè)計兩條引物(同一方向,,對同一單鏈模版),,一條包含計劃定點突變的序列,另一條引物包含質(zhì)粒上某一個單酶切位點,,不過在單酶切位點中引入突變,,這樣兩條引物除了所包含的突變位點,其他序列和質(zhì)粒上對應(yīng)位置的序列*一致,,退火后和質(zhì)粒模版結(jié)合,,通過T4 DNA聚合酶延伸,延伸反應(yīng)持續(xù)直到碰到另一條引物停止,,兩段包含突變位點的延伸產(chǎn)物經(jīng)T4連接成環(huán),,和模版鏈組成雜和環(huán),帶有兩處錯配,。單酶切反應(yīng)產(chǎn)物,,直接轉(zhuǎn)化Ecoli BMH 71-18 mutS(錯配修復(fù)缺陷株)。原來的雙鏈質(zhì)粒模版被切開而不能轉(zhuǎn)化,,而雜和質(zhì)粒由于一條鏈上單酶切位點引入突變而不被切開,,保持環(huán)狀質(zhì)粒得以轉(zhuǎn)化。轉(zhuǎn)化子的雜和雙鏈在E.coli的復(fù)制過程中分開,,再經(jīng)過一輪提質(zhì)粒,、單酶切、轉(zhuǎn)化,,zui后得到純和的突變質(zhì)粒,。這個試劑盒則是利用改造單酶切位點使得新合成的突變質(zhì)粒不被切開從而除去原來的模版質(zhì)粒。
有的時候研究可能需要多個位點的定點突變,,比如改造酶的活性或者動力學(xué)特性,,研究蛋白之間的相互作用位點等,單點突變不能滿足實驗的需要,,重復(fù)進行單點突變也非常浪費時間,。因而Stratagene公司又推出了QuikChange Multi Site-Directed Mutagenesis kit。zui多一次實驗可以引入5個定點突變,。這個試劑盒的原理和Clontech的相似,,就是準備多個帶突變的引物(同方向,,對同一單鏈模版),,退火后全部突變引物(不超過5個)都結(jié)合在同一環(huán)狀單鏈模版,PfuTurbo聚合酶延伸,,碰到下一個引物就停止,,各片斷經(jīng)連接成環(huán),,和單鏈模版組成雜和環(huán),DpnI消化雙鏈模版,,也消化雜和環(huán)中的模版,,只留下新合成的帶多個突變的單鏈環(huán)(mutant ssDNA),得以轉(zhuǎn)化E.coli,,形成雙鏈質(zhì)粒,。資料表明,引入3個定點突變的效率為60%,,5個定點突變的效率為30%,。得到的其他質(zhì)粒是帶有較少定點突變的質(zhì)粒,以引入3個定點突變?yōu)槔?,就是?0% 左右的轉(zhuǎn)化質(zhì)粒是帶有1-2個不同定點突變的質(zhì)粒(因為存在1-2個引物結(jié)合模版延伸形成單鏈環(huán)的可能),。
流程
定點突變一般須有含有待突變基因的高純度質(zhì)粒,不少于10μg,,電泳圖清晰,,達酶切及測序要求;
1.對待突變基因測序結(jié)果進行分析,設(shè)計突變方案;
2.根據(jù)突變方案設(shè)計合成覆蓋突變位點的雙向引物,,合成目的DNA兩端引物,,進行高保真PCR反應(yīng);
3.默認情況下,將PCR產(chǎn)物克隆至T載,,或者根據(jù)要求亞克隆至目的載體;DNA測序驗證突變序列的正確性,。
定點突變適用于蛋白結(jié)構(gòu)已有初步了解的基因,比PCR隨機突變更有目的性,,也更為,,簡單,同時改造基因更加"隨心所欲",。由于定點突變技術(shù)在蛋白質(zhì)組學(xué)中有這非常廣泛的應(yīng)用前景,,相信這個技術(shù)在不遠的將來還會有更大的改進和發(fā)展,也必將為更多人熟悉應(yīng)用,。

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