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Purifying Plasmid DNA from Bacterial Colonies Using the Qiagen Miniprep Kit

机译:使用Qiagen Miniprep试剂盒从细菌菌落中纯化质粒DNA

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摘要

Plasmid DNA purification from E. coli is a core technique for molecular cloning. Small scale purification (miniprep) from less than 5 ml of bacterial culture is a quick way for clone verification or DNA isolation, followed by further enzymatic reactions (polymerase chain reaction and restriction enzyme digestion). Here, we video-recorded the general procedures of miniprep through the QIAGEN's QIAprep 8 Miniprep Kit, aiming to introducing this highly efficient technique to the general beginners for molecular biology techniques. The whole procedure is based on alkaline lysis of E. coli cells followed by adsorption of DNA onto silica in the presence of high salt. It consists of three steps: 1) preparation and clearing of a bacterial lysate, 2) adsorption of DNA onto the QIAprep membrane, 3) washing and elution of plasmid DNA. All steps are performed without the use of phenol, chloroform, CsCl, ethidium bromide, and without alcohol precipitation. It usually takes less than 2 hours to finish the entire procedure.
机译:从大肠杆菌中纯化质粒DNA是分子克隆的核心技术。从少于5 ml的细菌培养物中进行小规模纯化(miniprep)是克隆验证或DNA分离的快速方法,然后进行进一步的酶促反应(聚合酶链反应和限制性酶切消化)。在这里,我们通过QIAGEN的QIAprep 8 Miniprep Kit录制了miniprep的一般步骤,旨在将这种高效技术引入分子生物学技术的一般初学者。整个过程基于大肠杆菌细胞的碱裂解,然后在高盐存在下将DNA吸附到硅胶上。它包括三个步骤:1)制备和清除细菌裂解液,2)DNA吸附在QIAprep膜上,3)洗涤和洗脱质粒DNA。所有步骤均在不使用苯酚,氯仿,CsCl,溴化乙锭且没有醇沉淀的情况下进行。通常只需不到2个小时即可完成整个过程。

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