Hotstart Taq酶資料說明

英文名稱：Hotstart Taq DNA Polymerase
其他名稱：Hotstart Taq DNA聚合酶
分子量：94kDa，單體
級別：BR
純度：≥99%
濃度：5u/ul 
活性定義：在74℃、30分鐘內，使10nmol脫氧核糖核酸合成滲入多聚核苷酸（吸附在DE-81上）所需的酶量
酶活性分析混合物：25mM TAPS(PH9.3,25℃), 50mM KC1, 2mM MgCL2, 0.2mM各種dATP,dGTP,dTTP, 0.1mM dCTP, 0.75mM活化的鮭魚精DNA和0.4MBq/ML(3H).-dTTP
保存緩沖液組分：20mM Tris-HCL(PH9.0), 1mM DTT, 0.1mM EDTA,100mM KC1, 0.5%(V/V) Tween 20，0.5%(v/v) Nonidet P40和50%(v/v)甘油
10×Hot start PCR Buffer：200mM Tris-HCL(PH8.3,25℃), 200mM KC1, 50mM (NH4)2SO4
抑制劑：陰離子去污劑（脫氧膽酸、肌氨酰和SDS的濃度分別高于0.06、0.02和0.01%時）
失活：酚/氯仿抽提
質量控制：相關測試表明無內切或外切脫氧核糖核酸酶、核糖核酸酶污染
功能啟動：熱啟動PCR
性狀(以下信息僅供參考)：液體。設計用于增強DNA擴增的特異性、敏感性和產量。使用該酶可在室溫配制反應體系，使用方便。它是一種化學修飾的重組Taq DNA Polymerase，蛋白分子氨基酸殘基上增加了熱不穩定的封閉基團。該酶在室溫下沒有活性，避免形成引物二聚體和非特異性延伸，從而增加DNA擴增的特異性。95℃加熱4分鐘可恢復活性。活化的酶具有與Taq DNA Polymerase相同的功能：催化5——3方向合成DNA，無可檢測的3——5校正外切酶活性，具有較低的5——3外切酶活性。該酶還具有脫氧核糖核酸酶轉移活性，在PCR產物的3-端多加11個腺嘌呤，活化前檢測不到這些活性。
用途：本品僅供科研，不得用于其它用途。(以下用途僅供參考)高產量擴增復雜模板；PCR特異性高-降低錯配效應和減少引物二聚體的生成；增強的PCR敏感性；使用方便，室溫配制PCR反應體系；擴增產物具有3-dA突出末端；熱啟動PCR；高產量擴增長達3kb片段；RT-PCR；特異性擴增復雜cDNA和基因組模板；擴增低拷貝DNA模板；實時PCR；多重PCR；制備TA克隆用PCR產物
保存：-20℃，保質期1年
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