pL1E-hc vector (V005101)

Basic Vector Information

Vector Name:
pL1E-hc
Antibiotic Resistance:
Ampicillin
Length:
5426 bp
Type:
Cloning vector
Replication origin:
ori
Source/Author:
Hochrein L, Machens F, Gremmels J, Schulz K, Messerschmidt K, Mueller-Roeber B.
Promoter:
SNR52

pL1E-hc vector Vector Map

pL1E-hc5426 bp60012001800240030003600420048005400oriAmpR2u oriSNR52 promotergRNA scaffoldSUP4 terminatorCYC1 terminatorI-SceI; cleavage sitehomology region E0*TRP1homology region F0*I-SceI; cleavage site

pL1E-hc vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       40924_27459        5426 bp DNA     circular SYN 18-DEC-2018
DEFINITION  Cloning vector pL1E-hc, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 5426)
  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 5426)
  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 5426)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 5426)
  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..5426
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     rep_origin      complement(64..652)
                     /direction=LEFT
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     CDS             complement(826..1683)
                     /label=AmpR
                     /note="beta-lactamase"
     rep_origin      complement(2367..3247)
                     /direction=LEFT
                     /label=2u ori
                     /note="yeast 2u plasmid origin of replication"
     promoter        3499..3767
                     /label=SNR52 promoter
                     /note="promoter for the S. cerevisiae small nucleolar RNA
                     gene SNR52"
     misc_RNA        3776..3850
                     /label=gRNA scaffold
                     /note="guide RNA scaffold for the Streptococcus pyogenes 
                     CRISPR/Cas9 system"
     terminator      3855..3874
                     /label=SUP4 terminator
                     /note="transcription terminator for the S. cerevisiae SUP4
                     tRNA gene"
     terminator      3926..4115
                     /label=CYC1 terminator
                     /note="transcription terminator for CYC1"
     misc_feature    4334..4351
                     /note="I-SceI; cleavage site"
     misc_feature    4352..4401
                     /label=homology region E0*
                     /note="homology region E0*"
     CDS             4410..5081
                     /label=TRP1
                     /note="phosphoribosylanthranilate isomerase, required for 
                     tryptophan biosynthesis"
     misc_feature    5181..5230
                     /label=homology region F0*
                     /note="homology region F0*"
     misc_feature    5231..5248
                     /note="I-SceI; cleavage site"

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