英语翻译本文通过PCR、转化、提质粒、酶切、连主要接、纯化等步骤构建了质粒pET28a-NULP1.先通过PCR扩增出了nulp1,并将nulp1连接入pMD18-T载体酶切检测并测序,得到正确的nulp1,再将nulp1连接到pET-28a载体,成功构建了pET-28a-NULP1重组质粒.1楼你纯粹是GOOGLE复制

本文通过PCR、转化、提质粒、酶切、连主要接、纯化等步骤构建了质粒pET28a-NULP1。先通过PCR扩增出了nulp1，并将nulp1连接入pMD18-T载体酶切检测并测序，得到正确的nulp1，再将nulp1连接到pET-28a载体，成功构建了pET-28a-NULP1重组质粒。
In this paper, PCR, transformation, reference plasmid, digestion, even the main access, purification steps, such as the construction of plasmid pET28a-NULP1. First PCR amplified through nulp1, and connect nulp1 into pMD18-T vector and sequenced enzyme detection, the correct nulp1, and then connect to nulp1 vector pET-28a, was successfully constructed pET-28a-NULP1 the reorganization of the quality tablets.

This aritcle through the steps such as PCR,transformation,distilling plasmid,EcoRI,connecting main links,purification and so on,in order to built the plasmid pET28a-NULP1.First,amplifing the nulp1 thr...