pTARBAC1 plasmid vector细菌人工染色体质粒载体 BioVector NTCC质粒载体菌种细胞基因保藏中心
- 价 格:¥98965
- 货 号:pTARBAC1
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
- 联系人:Dr.Xu, Biovector NTCC Inc.
电话:400-800-2947 工作QQ:1843439339 (微信同号)
邮件:Biovector@163.com
手机:18901268599
地址:北京
- 已注册
pTARBAC1 plasmid vector细菌人工染色体质粒载体
a new hybrid vector,pTARBAC1, containing a yeast artificial chromosome (YAC) cassette (a yeast selectablemarker and a centromere). The cassette allows transferring of BACs into yeast for their further modification. Furthermore, the new hybrid vector provides the opportunity to re-isolateeach DNA insert without construction of a new library of random clones. Digestion of a BACDNA by an endonuclease that has no recognition site in the vector, but which deletes mostof the internal insert sequence and leaves the unique flanking sequences, converts a BAC intoa TAR vector, thus allowing direct gene isolation. Cotransformation of a TAR vector andgenomic DNA into yeast spheroplasts, and subsequent recombination between the TAR vector’s flanking ends and a specific genomic fragment, allows rescue of the fragment as a circular YAC/BAC molecule. Here we prove a new cloning strategy by re-isolation of randomlychosen genomic fragments of different size from T. brucei cloned in BACs.
Supplier来源:BioVector NTCC Inc.
TEL电话:400-800-2947
Website网址: http://www.biovector.net
a new hybrid vector,pTARBAC1, containing a yeast artificial chromosome (YAC) cassette (a yeast selectablemarker and a centromere). The cassette allows transferring of BACs into yeast for their further modification. Furthermore, the new hybrid vector provides the opportunity to re-isolateeach DNA insert without construction of a new library of random clones. Digestion of a BACDNA by an endonuclease that has no recognition site in the vector, but which deletes mostof the internal insert sequence and leaves the unique flanking sequences, converts a BAC intoa TAR vector, thus allowing direct gene isolation. Cotransformation of a TAR vector andgenomic DNA into yeast spheroplasts, and subsequent recombination between the TAR vector’s flanking ends and a specific genomic fragment, allows rescue of the fragment as a circular YAC/BAC molecule. Here we prove a new cloning strategy by re-isolation of randomlychosen genomic fragments of different size from T. brucei cloned in BACs.
Supplier来源:BioVector NTCC Inc.
TEL电话:400-800-2947
Website网址: http://www.biovector.net
- 公告/新闻