Basic Vector Information
- Vector Name:
- pRED419-Amp
- Antibiotic Resistance:
- Ampicillin
- Length:
- 5401 bp
- Type:
- Gateway recycling vector
- Replication origin:
- ori
- Source/Author:
- Kimura T, Nakao A, Murata S, Kobayashi Y, Tanaka Y, Shibahara K, Kawazu T, Nakagawa T.
pRED419-Amp vector Map
pRED419-Amp vector Sequence
LOCUS 40924_36473 5401 bp DNA circular SYN 18-DEC-2018 DEFINITION Gateway recycling vector pRED419-Amp DNA, complete sequence. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 5401) AUTHORS Kimura T, Nakao A, Murata S, Kobayashi Y, Tanaka Y, Shibahara K, Kawazu T, Nakagawa T. TITLE Development of the gateway recycling cloning system for multiple linking of expression cassettes in a defined order, and direction on gateway compatible binary vectors JOURNAL Biosci. Biotechnol. Biochem. 77 (2), 430-434 (2013) PUBMED 23391940 REFERENCE 2 (bases 1 to 5401) AUTHORS Kimura T, Shibahara K, Tanaka Y, Nakao A, Kawazu T, Nakagawa T. TITLE Direct Submission JOURNAL Submitted (02-OCT-2012) Contact:Tsuyoshi Nakagawa Shimane University, Center for Integrated Research in Science; 1060 Nishikawatsu, Matsue, Shimane 690-8504, Japan REFERENCE 3 (bases 1 to 5401) TITLE Direct Submission REFERENCE 4 (bases 1 to 5401) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Biosci. Biotechnol. Biochem."; date: "2013"; volume: "77"; issue: "2"; pages: "430-434" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (02-OCT-2012) Contact:Tsuyoshi Nakagawa Shimane University, Center for Integrated Research in Science; 1060 Nishikawatsu, Matsue, Shimane 690-8504, Japan" COMMENT SGRef: number: 3; type: "Journal Article" COMMENT constructed using pDONR201. FEATURES Location/Qualifiers source 1..5401 /mol_type="other DNA" /organism="synthetic DNA construct" protein_bind 28..127 /label=attL1 /note="recombination site for the Gateway(R) LR reaction" primer_bind 159..175 /label=M13 rev /note="common sequencing primer, one of multiple similar variants" misc_feature complement(188..244) /label=MCS /note="pUC18/19 multiple cloning site" primer_bind complement(245..261) /label=M13 fwd /note="common sequencing primer, one of multiple similar variants" protein_bind 803..927 /label=attR4 /note="recombination site for the Gateway(R) LR reaction" promoter 952..982 /label=lac UV5 promoter /note="E. coli lac promoter with an 'up' mutation" misc_feature 1254..1294 /label=rare cutter sites /note="rare cutter sites" promoter 1325..1429 /label=AmpR promoter CDS 1430..2287 /codon_start=1 /label=AmpR /note="beta-lactamase" /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRVDAGQEQLGRRIHYSQNDLVEYS PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW EPELNEAIPNDERDTTMPAAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS LIKHW" protein_bind complement(2645..2768) /label=attR3 /note="recombination site for the Gateway(R) LR reaction" protein_bind complement(3274..3373) /label=attL2 /note="recombination site for the Gateway(R) LR reaction" CDS 3496..4302 /codon_start=1 /label=KanR /note="aminoglycoside phosphotransferase" /translation="MSHIQRETSRPRLNSNMDADLYGYKWARDNVGQSGATIYRLYGKP DAPELFLKHGKGSVANDVTDEMVRLNWLTEFMPLPTIKHFIRTPDDAWLLTTAIPGKTA FQVLEEYPDSGENIVDALAVFLRRLHSIPVCNCPFNSDRVFRLAQAQSRMNNGLVDASD FDDERNGWPVEQVWKEMHKLLPFSPDSVVTHGDFSLDNLIFDEGKLIGCIDVGRVGIAD RYQDLAILWNCLGEFSPSLQKRLFQKYGIDNPDMNKLQFHLMLDEFF" rep_origin 4448..5036 /direction=RIGHT /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" terminator complement(5171..5198) /label=rrnB T2 terminator /note="transcription terminator T2 from the E. coli rrnB gene" terminator complement(5290..5376) /label=rrnB T1 terminator /note="transcription terminator T1 from the E. coli rrnB gene"
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