Basic Vector Information
- Vector Name:
- pQE30NST
- Antibiotic Resistance:
- Ampicillin
- Length:
- 3494 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Bussow K, Cahill D, Nietfeld W, Bancroft D, Scherzinger E, Lehrach H, Walter G.
- Promoter:
- T5
pQE30NST vector Map
pQE30NST vector Sequence
LOCUS 40924_36178 3494 bp DNA circular SYN 18-DEC-2018 DEFINITION Cloning vector pQE30NST, complete sequence. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 3494) AUTHORS Bussow K, Cahill D, Nietfeld W, Bancroft D, Scherzinger E, Lehrach H, Walter G. TITLE A method for global protein expression and antibody screening on high-density filters of an arrayed cDNA library JOURNAL Nucleic Acids Res. 26 (21), 5007-5008 (1998) PUBMED 9776767 REFERENCE 2 (bases 1 to 3494) AUTHORS Bussow K, Cahill D, Nietfeld W, Bancroft D, Scherzinger E, Lehrach H, Walter G, Doebeli H, Eggimann B, Gentz R, Hochuli E, Stueber D. TITLE Direct Submission JOURNAL Submitted (25-JUN-1998) Lehrach, Max-Planck-Institut fuer Molekulare Genetik, Ihnestrasse 73, Berlin 14195, Germany REFERENCE 3 (bases 1 to 3494) TITLE Direct Submission REFERENCE 4 (bases 1 to 3494) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Nucleic Acids Res."; date: "1998"; volume: "26"; issue: "21"; pages: "5007-5008" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (25-JUN-1998) Lehrach, Max-Planck-Institut fuer Molekulare Genetik, Ihnestrasse 73, Berlin 14195, Germany" COMMENT SGRef: number: 3; type: "Journal Article" FEATURES Location/Qualifiers source 1..3494 /mol_type="other DNA" /organism="synthetic DNA construct" promoter 10..54 /label=T5 promoter /note="bacteriophage T5 promoter for E. coli RNA polymerase, with embedded lac operator" protein_bind 62..78 /label=lac operator /bound_moiety="lac repressor encoded by lacI" /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)." RBS 97..108 /note="strong bacterial ribosome binding site (Elowitz and Leibler, 2000)" regulatory 101..107 /regulatory_class="ribosome_binding_site" misc_feature 115 /note="translation start site for inserts cloned into the multiple cloning site" CDS 127..144 /label=6xHis /note="6xHis affinity tag" promoter 152..170 /label=SP6 promoter /note="promoter for bacteriophage SP6 RNA polymerase" promoter complement(201..219) /label=T7 promoter /note="promoter for bacteriophage T7 RNA polymerase" terminator 240..334 /label=lambda t0 terminator /note="transcription terminator from phage lambda" CDS 378..1034 /label=CmR /note="chloramphenicol acetyltransferase" terminator 1102..1188 /label=rrnB T1 terminator /note="transcription terminator T1 from the E. coli rrnB gene" misc_feature 1344..1484 /label=bom /note="basis of mobility region from pBR322" rep_origin complement(1670..2258) /direction=LEFT /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" CDS complement(2432..3289) /label=AmpR /note="beta-lactamase" promoter complement(3290..3394) /label=AmpR promoter
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