pL1B-hc vector (V005107)

Basic Vector Information

Vector Name:
pL1B-hc
Antibiotic Resistance:
Ampicillin
Length:
5851 bp
Type:
Cloning vector
Replication origin:
ori
Source/Author:
Hochrein L, Machens F, Gremmels J, Schulz K, Messerschmidt K, Mueller-Roeber B.
Promoter:
SNR52

pL1B-hc vector Vector Map

pL1B-hc5851 bp60012001800240030003600420048005400oriAmpR2u oriSNR52 promotergRNA scaffoldSUP4 terminatorCYC1 terminatorI-SceI; cleavage sitehomology region B0*LEU2homology region C0*I-SceI; cleavage site

pL1B-hc vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       40924_27429        5851 bp DNA     circular SYN 18-DEC-2018
DEFINITION  Cloning vector pL1B-hc, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 5851)
  AUTHORS   Hochrein L, Machens F, Gremmels J, Schulz K, Messerschmidt K, 
            Mueller-Roeber B.
  TITLE     AssemblX: a user-friendly toolkit for rapid and reliable multi-gene 
            assemblies
  JOURNAL   Nucleic Acids Res. (2017) In press
  PUBMED    28130422
REFERENCE   2  (bases 1 to 5851)
  AUTHORS   Hochrein L, Machens F, Gremmels J, Schulz K, Messerschmidt K, 
            Mueller-Roeber B.
  TITLE     Direct Submission
  JOURNAL   Submitted (11-NOV-2016) Department of Molecular Biology - Cell2Fab 
            research unit, University of Potsdam, Karl-Liebknecht-Str. 24-25, 
            Potsdam, Brandenburg 14476, Germany
REFERENCE   3  (bases 1 to 5851)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 5851)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: "Nucleic 
            Acids Res. (2017) In press"
COMMENT     SGRef: number: 2; type: "Journal Article"; journalName: "Submitted 
            (11-NOV-2016) Department of Molecular Biology - Cell2Fab research 
            unit, University of Potsdam, Karl-Liebknecht-Str. 24-25, Potsdam, 
            Brandenburg 14476, Germany"
COMMENT     SGRef: number: 3; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..5851
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     rep_origin      complement(61..649)
                     /direction=LEFT
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     CDS             complement(823..1680)
                     /label=AmpR
                     /note="beta-lactamase"
     rep_origin      complement(2364..3244)
                     /direction=LEFT
                     /label=2u ori
                     /note="yeast 2u plasmid origin of replication"
     promoter        3496..3764
                     /label=SNR52 promoter
                     /note="promoter for the S. cerevisiae small nucleolar RNA
                     gene SNR52"
     misc_RNA        3773..3847
                     /label=gRNA scaffold
                     /note="guide RNA scaffold for the Streptococcus pyogenes 
                     CRISPR/Cas9 system"
     terminator      3852..3871
                     /label=SUP4 terminator
                     /note="transcription terminator for the S. cerevisiae SUP4
                     tRNA gene"
     terminator      3923..4112
                     /label=CYC1 terminator
                     /note="transcription terminator for CYC1"
     misc_feature    4331..4348
                     /note="I-SceI; cleavage site"
     misc_feature    4349..4398
                     /label=homology region B0*
                     /note="homology region B0*"
     CDS             4407..5498
                     /label=LEU2
                     /note="3-isopropylmalate dehydrogenase, required for
                     leucine biosynthesis"
     misc_feature    5603..5652
                     /label=homology region C0*
                     /note="homology region C0*"
     misc_feature    5653..5670
                     /note="I-SceI; cleavage site"

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