Churchward G, Belin D, Nagamine Y
Gene. 1984 Nov;31(1-3):165-71. doi: 10.1016/0378-1119(84)90207-5.
We have constructed a plasmid cloning vector, pGB2, which is derived from the Escherichia coli plasmid pSC101. The plasmid, which specifies resistance to spectinomycin and streptomycin, contains unique restriction sites for the enzymes HindIII, PstI, SalI, BamHI, SmaI and EcoRI. pGB2 shows no sequence homology, as detected by DNA-DNA hybridization, to several widely used vectors such as pBR322, pUC8 and phage lambda L47.1. Amongst other applications, DNA fragments can be cloned into the plasmid and then radioactive plasmid DNA can be used as a probe to screen recombinant DNA libraries.
我们构建了一种质粒克隆载体pGB2,它源自大肠杆菌质粒pSC101。该质粒赋予对壮观霉素和链霉素的抗性,含有HindIII、PstI、SalI、BamHI、SmaI和EcoRI等酶的独特限制性酶切位点。通过DNA-DNA杂交检测发现,pGB2与几种广泛使用的载体如pBR322、pUC8和噬菌体λL47.1没有序列同源性。在其他应用中,DNA片段可克隆到该质粒中,然后放射性质粒DNA可作为探针用于筛选重组DNA文库。