Basic Vector Information
- Vector Name:
- pKW3_MB1Amp_TracrK_Spacer
- Antibiotic Resistance:
- Ampicillin
- Length:
- 3246 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Wang K, de la Torre D, Robertson WE, Chin JW.
- Promoter:
- PLtetO-1
pKW3_MB1Amp_TracrK_Spacer vector Map
pKW3_MB1Amp_TracrK_Spacer vector Sequence
LOCUS 62056_13610 3246 bp DNA circular SYN 30-AUG-2019 DEFINITION Cloning vector pKW3_MB1Amp_TracrK_Spacer, complete sequence. ACCESSION MN226641 VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 3246) AUTHORS Wang K, de la Torre D, Robertson WE, Chin JW. TITLE Programmed chromosome fission and fusion enable precise large-scale genome rearrangement and assembly JOURNAL Science 365 (6456), 922-926 (2019) REFERENCE 2 (bases 1 to 3246) AUTHORS Wang K, de la Torre D, Robertson WE, Chin JW. TITLE Direct Submission JOURNAL Submitted (24-JUL-2019) Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, Cambridgeshire CB2 0QH, United Kingdom REFERENCE 3 (bases 1 to 3246) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Science"; date: "2019"; volume: "365"; issue: "6456"; pages: "922-926" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (24-JUL-2019) Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, Cambridgeshire CB2 0QH, United Kingdom" COMMENT ##Assembly-Data-START## Sequencing Technology :: Sanger dideoxy sequencing ##Assembly-Data-END## FEATURES Location/Qualifiers source 1..3246 /mol_type="other DNA" /organism="synthetic DNA construct" promoter 104..208 /label=AmpR promoter CDS 209..1066 /label=AmpR /note="beta-lactamase" rep_origin 1240..1828 /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" terminator complement(1992..2078) /label=rrnB T1 terminator /note="transcription terminator T1 from the E. coli rrnB gene" regulatory 2234..2268 /label=Cas9 promoter predicted /note="Cas9 promoter predicted" /regulatory_class="promoter" regulatory 2300..2327 /label=putative tracrRNA promoter /note="putative tracrRNA promoter" /regulatory_class="promoter" misc_RNA 2381..2459 /label=tracrRNA /note="trans-activating CRISPR RNA for the Streptococcus pyogenes CRISPR/Cas9 system" misc_feature 2571..2702 /label=crRNA leader /note="crRNA leader sequence for the Streptococcus pyogenes CRISPR/Cas system" repeat_region 2703..2738 /label=DR /note="direct repeat for the Streptococcus pyogenes CRISPR/Cas system" gap 2739..2768 /estimated_length=30 gap 2805..2834 /estimated_length=30 gap 2871..2900 /estimated_length=30 gap 2937..2966 /estimated_length=30 gap 3003..3032 /estimated_length=30 gap 3069..3098 /estimated_length=30 promoter complement(3167..3240) /label=PLtetO-1 promoter /note="modified phage lambda PL promoter with tet operator sites (Lutz and Bujard, 1997)"
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