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foreign genes and its application for the generation of LC16m8-based vaccines against herpes simplex virus 2 JOURNAL Unpublished REFERENCE 2 (bases 1 to 3671) AUTHORS Yoshikawa T, Saijo M. TITLE Direct Submission JOURNAL Submitted (27-SEP-2017) Contact:Tomoki Yoshikawa National Institute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 TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Unpublished" SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (27-SEP-2017) Contact:Tomoki Yoshikawa National Institute of Infectious Diseases,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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