pPIBT7 vector (V004108)

Basic Vector Information

Vector Name:
pPIBT7
Antibiotic Resistance:
Ampicillin
Length:
4471 bp
Type:
Transformation vector
Replication origin:
ori
Source/Author:
Oertel W, Weissgerber A.

pPIBT7 vector Vector Map

pPIBT74471 bp600120018002400300036004200Ulva mutabilis RbcS promoterUlva mutabilis RbcS intron 1; enhancerUlva mutabilis RbcS terminatorM13 fwdAmpR promoterAmpRoriCAP binding sitelac promoterlac operatorM13 rev

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 ℃.

pPIBT7 vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       40924_34480        4471 bp DNA     circular SYN 18-DEC-2018
DEFINITION  Transformation vector pPIBT7, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 4471)
  AUTHORS   Oertel W, Weissgerber A.
  TITLE     Transformation of Ulva mutabilis Foyn with plasmids integrating into
            the chromosome
  JOURNAL   Unpublished
REFERENCE   2  (bases 1 to 4471)
  AUTHORS   Oertel W, Weissgerber A.
  TITLE     Direct Submission
  JOURNAL   Submitted (25-SEP-2007) Biochemistry, Genetics and Microbiology, 
            Division of Genetics, University of Regensburg, Universitaetsstr. 
            31, Regensburg, Bavaria 93053, Germany
REFERENCE   3  (bases 1 to 4471)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 4471)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: 
            "Unpublished"
COMMENT     SGRef: number: 2; type: "Journal Article"; journalName: "Submitted 
            (25-SEP-2007) Biochemistry, Genetics and Microbiology, Division of 
            Genetics, University of Regensburg, Universitaetsstr. 31, 
            Regensburg, Bavaria 93053, Germany"
COMMENT     SGRef: number: 3; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..4471
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     regulatory      1..546
                     /label=Ulva mutabilis RbcS promoter
                     /note="Ulva mutabilis RbcS promoter"
                     /regulatory_class="promoter"
     intron          555..1051
                     /gene="ble"
                     /note="Ulva mutabilis RbcS intron 1; enhancer"
     CDS             1050..1415
                     /label=BleoR
                     /note="antibiotic-binding protein"
     regulatory      1419..1807
                     /label=Ulva mutabilis RbcS terminator
                     /note="Ulva mutabilis RbcS terminator"
                     /regulatory_class="terminator"
     primer_bind     complement(1834..1850)
                     /label=M13 fwd
                     /note="common sequencing primer, one of multiple similar 
                     variants"
     promoter        2324..2428
                     /label=AmpR promoter
     CDS             2429..3286
                     /label=AmpR
                     /note="beta-lactamase"
     rep_origin      3460..4048
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     protein_bind    4336..4357
                     /label=CAP binding site
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     promoter        4372..4402
                     /label=lac promoter
                     /note="promoter for the E. coli lac operon"
     protein_bind    4410..4426
                     /label=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)."
     primer_bind     4434..4450
                     /label=M13 rev
                     /note="common sequencing primer, one of multiple similar 
                     variants"

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