pIC19H

质粒编号:
质粒名称: pIC19H
其他名称:
质粒大小（bp）: 2701
抗性: Ampicillin
质粒类型: Unspecified
是否病毒: Unspecified
启动子:
稳转或瞬转: Unspecified
组成型或诱导性: Unspecified
表达水平:
蛋白标签:
测序引物:
GenBank号: L08910
其他属性: These data and their annotation were supplied to GenBank by Will Gilbert under the auspices of the GenBank Currator Program. Assembled from pUC9 and pIC7 by F. Pfeiffer For construction of pIC7, a synthetic oligonucleotide has been used to replace the pUC8 polylinker and thus to construct a new cloning vector with a different polylinker. The other pIC-vectors are based on this new pIC7 polylinker, which was combined with the existing pUC9 and pUC19 polylinkers in the following arrangements: pIC19 and pICEM19 vectors: pIC19R: EcoRI- Poly (pIC7) -HindIII- Poly (pUC9) -EcoRI pIC19H: HindIII- Poly (pUC9) -EcoRI – Poly (pIC7) -HindIII pIC20-vectors: pIC20R: EcoRI- Poly (pIC7) -HindIII- Poly(pUC19) -EcoRI pIC20H: HindIII- Poly(pUC19) -EcoRI – Poly (pIC7) -HindIII To produce greater versatility of insertional inactivation of beta-galactosidase activity for subcloning and sequencing, a chemically synthesized oligonucleotide, specifying nine restriction sites including BglII, XhoI, NruI, ClaI, SacI and EcorV in various configurations with existing polylinkers, was created. These improved polylinkers were inserted into plasmids for routine cloning of ds-DNA and into chimeric phage/plasmids for biological production of ss-DNA. The most versatile polyrecognition pattern specifies 17 restriction sites in the beta-galactosidase alpha-complementing gene fragment. Clone pIC7 was used to produce all the other polylinker-carrying vectors. A general purpose plasmid vector with a polylinker containing 13 sites in lacZ'. Medium is 1227 LB plus ampicillin. Hosts: E.coli TB1, E.coli, E.coli JM83. Related vectors: pIC7, pUC9, pIC19R.
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