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【质粒图谱】pIC19H质粒图谱及相关信息



【质粒图谱】pIC19H质粒图谱及相关信息

 

pIC19H图谱及相信息

图谱库IDG0667

粒名: pIC19H

关说明: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.

pIC19H图谱

 

特征序列位:

M13_forward20_primer

 

321 - 305

lacZ_a

 

314 - 457

M13_pUC_fwd_primer

 

336 - 314

AmpR_promoter

 

830 - 858

pGEX_3_primer

 

649 - 671

M13_reverse_primer

 

206 - 224

M13_pUC_rev_primer

 

185 - 207

lac_promoter

 

142 - 171

Orf2

 

900 - 1760

Ampicillin

 

900 - 1760

pBR322_origin

 

1915 - 2534

 

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