Basic Vector Information
pUCP30T-GFPmut3 vector Vector Map
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 ℃.
pUCP30T-GFPmut3 vector Sequence
LOCUS 40924_45373 5168 bp DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pUCP30T-GFPmut3, complete sequence.
ACCESSION .
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 5168)
AUTHORS Barbier M, Damron FH.
TITLE Rainbow Vectors for Broad-Range Bacterial Fluorescence Labeling
JOURNAL PLoS ONE 11 (3), E0146827 (2016)
PUBMED 26937640
REFERENCE 2 (bases 1 to 5168)
AUTHORS Barbier M, Damron FH.
TITLE Direct Submission
JOURNAL Submitted (06-OCT-2015) Microbiology, Immunology and Cell Biology,
West Virginia University, School of Medicine, One Medical Center
Drive, Morgantown, WV 26506, USA
REFERENCE 3 (bases 1 to 5168)
TITLE Direct Submission
REFERENCE 4 (bases 1 to 5168)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "PLoS ONE";
date: "2016"; volume: "11"; issue: "3"; pages: "E0146827"
COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
(06-OCT-2015) Microbiology, Immunology and Cell Biology, West
Virginia University, School of Medicine, One Medical Center Drive,
Morgantown, WV 26506, USA"
COMMENT SGRef: number: 3; type: "Journal Article"
FEATURES Location/Qualifiers
source 1..5168
/mol_type="other DNA"
/organism="synthetic DNA construct"
rep_origin 72..660
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
oriT complement(732..840)
/direction=LEFT
/label=oriT
/note="incP origin of transfer"
protein_bind 1224..1245
/label=CAP binding site
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 1260..1290
/label=lac promoter
/note="promoter for the E. coli lac operon"
protein_bind 1298..1314
/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 1322..1338
/label=M13 rev
/note="common sequencing primer, one of multiple similar
variants"
RBS 1378..1389
/note="strong bacterial ribosome binding site (Elowitz and
Leibler, 2000)"
CDS 1396..2109
/label=yeGFP
/note="yeast-enhanced green fluorescent protein"
terminator 2132..2226
/label=lambda t0 terminator
/note="transcription terminator from phage lambda"
primer_bind complement(2273..2289)
/label=M13 fwd
/note="common sequencing primer, one of multiple similar
variants"
CDS complement(2453..3283)
/label=pRO1600 Rep
/note="replication protein for the broad-host-range plasmid
pRO1600 from Pseudomonas aeruginosa"
rep_origin 3297..3648
/label=pRO1600 oriV
/note="broad-host-range origin of replication from
Pseudomonas aeruginosa plasmid pRO1600; requires the
pRO1600 Rep protein for replication (West et al., 1994)"
promoter 3689..3717
/label=Pc promoter
/note="class 1 integron promoter"
CDS 3906..4436
/label=GmR
/note="gentamycin acetyltransferase"
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