Construction of T Vector Using Restriction Endonuclease XcmⅠ
doi: 10.15886/j.cnki.rdswxb.2010.03.002
- Received Date: 2010-07-13
Abstract: In our report,rice variety Nipponbare genome were used as template,a pair of primers which were added a XcmⅠ site at each 5’ end were used to amplify,and a 627bp fragments were obtained,which was ligated into pGEM-T Easy to develop a recombinant vector,T-xia. Self-made T vector was obtained when T-xia was digested by XcmⅠ,and the results of the ligation with other PCR products indicated that 80% recombination clones contained target fragments.
Citation: | XIA Zhi-hui, DONG Jun-mei, LUO Yue-hua. Construction of T Vector Using Restriction Endonuclease XcmⅠ[J]. Journal of Tropical Biology, 2010, 1(3): 206-209. doi: 10.15886/j.cnki.rdswxb.2010.03.002 |