Basic Vector Information
- Vector Name:
- pCR-Amp-mCherry-XGPRT
- Antibiotic Resistance:
- Ampicillin
- Length:
- 3671 bp
- Type:
- Expression vector
- Replication origin:
- ori
- Source/Author:
- Omura N, Yoshikawa T, Fujii H, Shibamura M
- Promoter:
- SP6
pCR-Amp-mCherry-XGPRT vector Map
pCR-Amp-mCherry-XGPRT vector Sequence
LOCUS V015707 3671 bp DNA circular SYN 02-APR-2020
DEFINITION Exported.
ACCESSION V015707
VERSION V015707
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 3671)
AUTHORS Omura N, Yoshikawa T, Fujii H, Shibamura M, Inagaki T, Kato H, Egawa
K, Harada S, Yamada S, Takeyama H, Saijo M.
TITLE A novel system for constructing a recombinant highly-attenuated
vaccinia virus strain (LC16m8) expressing foreign genes and its
application for the generation of LC16m8-based vaccines against
herpes simplex virus 2
JOURNAL Unpublished
REFERENCE 2 (bases 1 to 3671)
AUTHORS Yoshikawa T, Saijo M.
TITLE Direct Submission
JOURNAL Submitted (27-SEP-2017) Contact:Tomoki Yoshikawa National Institute
of Infectious Diseases, Department of Virology I; 1-23-1 Toyama,
Shinjuku-ku, Tokyo 162-8640, Japan URL
:https://www.niid.go.jp/niid/en/
REFERENCE 3 (bases 1 to 3671)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName:
"Unpublished"
SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
(27-SEP-2017) Contact:Tomoki Yoshikawa National Institute of
Infectious Diseases, Department of Virology I; 1-23-1 Toyama,
Shinjuku-ku, Tokyo 162-8640, Japan URL
:https://www.niid.go.jp/niid/en/"
FEATURES Location/Qualifiers
source 1..3671
/mol_type="other DNA"
/organism="synthetic DNA construct"
rep_origin complement(182..770)
/direction=LEFT
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
CDS complement(887..1744)
/label="AmpR"
/note="beta-lactamase"
promoter complement(1745..1815)
/label="AmpR promoter"
primer_bind 1951..1967
/label="M13 fwd"
/note="common sequencing primer, one of multiple similar
variants"
promoter 1974..1992
/label="T7 promoter"
/note="promoter for bacteriophage T7 RNA polymerase"
regulatory 2072..2111
/label="VAC early late promoter"
/note="VAC early late promoter"
/regulatory_class="promoter"
CDS 2112..2819
/label="mCherry"
/note="monomeric derivative of DsRed fluorescent protein
(Shaner et al., 2004)"
regulatory 2830..2869
/label="VAC early late promoter"
/note="VAC early late promoter"
/regulatory_class="promoter"
CDS 2876..3331
/gene="gpt"
/label="Xanthine-guanine phosphoribosyltransferase"
/note="Xanthine-guanine phosphoribosyltransferase from
Escherichia coli O17:K52:H18 (strain UMN026 / ExPEC).
Accession#: B7N8G9"
promoter complement(3415..3433)
/label="SP6 promoter"
/note="promoter for bacteriophage SP6 RNA polymerase"
primer_bind complement(3451..3467)
/label="M13 rev"
/note="common sequencing primer, one of multiple similar
variants"
protein_bind complement(3475..3491)
/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)."
promoter complement(3499..3529)
/label="lac promoter"
/note="promoter for the E. coli lac operon"
protein_bind complement(3544..3565)
/label="CAP binding site"
/note="CAP binding activates transcription in the presence
of cAMP."
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