pVP68K vector (V010566)

Basic Vector Information

Vector Name:
pVP68K
Antibiotic Resistance:
Chloramphenicol
Length:
6353 bp
Type:
Structural Genomics Vectors
Replication origin:
ori
Source/Author:
Blommel PG, Martin PA, Wrobel RL, Steffen E, Fox BG.
Selection Marker:
Neomycin/G418(Geneticin)
Copy Number:
High copy number
Promoter:
T5

pVP68K vector Vector Map

pVP68K6353 bp300600900120015001800210024002700300033003600390042004500480051005400570060006300T5 promoterlac operatorRBSATG8xHisMBPHRV 3C sitebarnaselac UV5 promoterCmRMCSattB2rrnB T1 terminatorCAP binding sitelacIlacI promoterbomoriNeoR/KanR

Plasmid Resuspension Protocol:

1. Centrifuge at 5,000×g for 5 min.

2. Carefully open the tube and add 20 μl of sterile water to dissolve the DNA.

3. Close the tube and incubate for 10 minutes at room temperature.

4. Briefly vortex the tube and then do a quick spin to concentrate the liquid at the bottom. Speed is less than 5000×g.

5.Store the plasmid at -20 ℃.

pVP68K vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       pVP68K.        6353 bp DNA     circular SYN 01-JAN-1980
DEFINITION  Bacterial Flexi(R) Vector with a kanamycin resistance marker, for 
            appending an N-terminal 8xHis-MBP-HRV 3C cassette to an expressed 
            protein.
ACCESSION   .
VERSION     .
KEYWORDS    pVP68K.
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 6353)
  AUTHORS   Blommel PG, Martin PA, Wrobel RL, Steffen E, Fox BG.
  TITLE     High efficiency single step production of expression plasmids from 
            cDNA clones using the Flexi Vector cloning system.
  JOURNAL   Protein Expr. Purif. 2006;47:562-70.
  PUBMED    16377204
REFERENCE   2  (bases 1 to 6353)
  AUTHORS   Center for Eukaryotic Structural Genomics
  TITLE     Direct Submission
REFERENCE   3  (bases 1 to 6353)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: "Protein 
            Expr. Purif."; date: "2006"; volume: "47"; pages: "562-70"
COMMENT     SGRef: number: 2; type: "Journal Article"
COMMENT     To remove the lethal barnase gene, insert an ORF between the SgfI 
            site and the PmeI site or a downstream site.
FEATURES             Location/Qualifiers
     source          1..6353
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     promoter        126..170
                     /label=T5 promoter
                     /note="bacteriophage T5 promoter for E. coli RNA
                     polymerase, with embedded lac operator"
     protein_bind    178..194
                     /label=lac repressor encoded by lacI binding site
                     /bound_moiety="lac repressor encoded by lacI"
                     /note="lac operator"
                     /note="The lac repressor binds to the lac operator to
                     inhibit transcription in E. coli. This inhibition can be 
                     relieved by adding lactose or 
                     isopropyl-beta-D-thiogalactopyranoside (IPTG)."
     RBS             217..222
                     /note="ribosome binding site"
     CDS             231..233
                     /codon_start=1
                     /product="start codon"
                     /label=start codon
                     /note="ATG"
                     /translation="M"
     CDS             237..260
                     /label=8xHis
                     /note="8xHis affinity tag"
     CDS             267..1364
                     /label=MBP
                     /note="maltose binding protein from E. coli"
     CDS             1389..1412
                     /label=HRV 3C site
                     /note="recognition and cleavage site for human rhinovirus
                     3C and PreScission proteases"
     CDS             1450..1782
                     /label=barnase
                     /note="ribonuclease from Bacillus amyloliquefaciens"
     promoter        1801..1831
                     /label=lac UV5 promoter
                     /note="E. coli lac promoter with an 'up' mutation"
     CDS             1885..2541
                     /label=CmR
                     /note="chloramphenicol acetyltransferase"
     misc_feature    2554..2609
                     /label=MCS
                     /note="pUC18/19 multiple cloning site"
     protein_bind    complement(2694..2714)
                     /label=attB2
                     /note="core recombination site for the Gateway(R) BP
                     reaction"
     terminator      2801..2887
                     /label=rrnB T1 terminator
                     /note="transcription terminator T1 from the E. coli rrnB
                     gene"
     protein_bind    complement(2946..2967)
                     /label=CAP binding site
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     CDS             complement(2983..4062)
                     /label=lacI
                     /note="lac repressor"
     promoter        complement(4063..4140)
                     /label=lacI promoter
     misc_feature    4293..4433
                     /label=bom
                     /note="basis of mobility region from pBR322"
     rep_origin      complement(4619..5207)
                     /direction=LEFT
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     CDS             complement(5388..6179)
                     /label=NeoR/KanR
                     /note="aminoglycoside phosphotransferase from Tn5"

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