Basic Vector Information
- Vector Name:
- p1cVTm
- Antibiotic Resistance:
- Ampicillin
- Length:
- 4013 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Boehm CR, Grant PK, Haseloff J.
p1cVTm 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 ℃.
p1cVTm vector Sequence
LOCUS 40924_2448 4013 bp DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector p1cVTm, complete sequence.
ACCESSION .
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 4013)
AUTHORS Boehm CR, Grant PK, Haseloff J.
TITLE Programmed hierarchical patterning of bacterial populations
JOURNAL Unpublished
REFERENCE 2 (bases 1 to 4013)
AUTHORS Boehm CR, Grant PK, Haseloff J.
TITLE Direct Submission
JOURNAL Submitted (21-FEB-2017) Plant Sciences, University of Cambridge,
Downing Street, Cambridge, Cambridgeshire CB2 3EA, United Kingdom
REFERENCE 3 (bases 1 to 4013)
TITLE Direct Submission
REFERENCE 4 (bases 1 to 4013)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName:
"Unpublished"
COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
(21-FEB-2017) Plant Sciences, University of Cambridge, Downing
Street, Cambridge, Cambridgeshire CB2 3EA, United Kingdom"
COMMENT SGRef: number: 3; type: "Journal Article"
COMMENT ##Assembly-Data-START##
Sequencing Technology :: Sanger dideoxy sequencing
##Assembly-Data-END##
FEATURES Location/Qualifiers
source 1..4013
/mol_type="other DNA"
/organism="synthetic DNA construct"
rep_origin complement(49..637)
/direction=LEFT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
regulatory 818..852
/label=PJ23101*
/note="PJ23101*"
/regulatory_class="promoter"
regulatory 861..878
/label=BBa_B0034
/note="BBa_B0034"
/regulatory_class="ribosome_binding_site"
RBS 861..872
/note="strong bacterial ribosome binding site (Elowitz and
Leibler, 2000)"
CDS 879..1595
/label=Venus
/note="yellow fluorescent protein (YFP) with fast and
efficient maturation (Nagai et al., 2002)"
terminator 1618..1689
/label=rrnB T1 terminator
/note="transcription terminator T1 from the E. coli rrnB
gene"
terminator 1705..1732
/label=T7Te terminator
/note="phage T7 early transcription terminator"
CDS complement(1748..2605)
/label=AmpR
/note="beta-lactamase"
promoter complement(2606..2710)
/label=AmpR promoter
terminator complement(2800..2843)
/label=bacterial terminator
/note="putative bacterial transcription terminator"
misc_feature 2846..2867
/label=BioBrick prefix
/note="BioBrick prefix for parts that do not start with
'ATG'"
terminator complement(2874..2901)
/label=T7Te terminator
/note="phage T7 early transcription terminator"
terminator complement(2917..2988)
/label=rrnB T1 terminator
/note="transcription terminator T1 from the E. coli rrnB
gene"
CDS complement(3011..3727)
/label=mTurquoise2
/note="enhanced monomeric variant of CFP (Goedhart et al.,
2012)"
regulatory complement(3728..3745)
/label=BBa_B0034
/note="BBa_B0034"
/regulatory_class="ribosome_binding_site"
RBS 3734..3745
/note="strong bacterial ribosome binding site (Elowitz and
Leibler, 2000)"
regulatory complement(3754..3788)
/label=PJ23101
/note="PJ23101"
/regulatory_class="promoter"
misc_feature 3789..3809
/label=BioBrick suffix
/note="universal suffix for all parts"
terminator 3810..3867
/label=his operon terminator
/note="This putative transcriptin terminator from the E.
coli his operon has a 2-bp deletion introduced during
synthesis. Its efficiency has not been determined."
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