pL1D-lc vector (V005102)

Basic Vector Information

Vector Name:
pL1D-lc
Antibiotic Resistance:
Ampicillin
Length:
8084 bp
Type:
Cloning vector
Replication origin:
ori
Source/Author:
Hochrein L, Machens F, Gremmels J, Schulz K, Messerschmidt K, Mueller-Roeber B.
Promoter:
SNR52

pL1D-lc vector Map

pL1D-lc8084 bp400800120016002000240028003200360040004400480052005600600064006800720076008000oriAmpRCEN/ARSSNR52 promotergRNA scaffoldSUP4 terminatorCYC1 terminatorI-SceI; cleavage sitehomology region D0*LYS2homology region E0*I-SceI; cleavage site

pL1D-lc vector Sequence

LOCUS       40924_27454        8084 bp DNA     circular SYN 18-DEC-2018
DEFINITION  Cloning vector pL1D-lc, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 8084)
  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 8084)
  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 8084)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 8084)
  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..8084
                     /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"
     misc_feature    complement(1778..2281)
                     /label=CEN/ARS
                     /note="S. cerevisiae CEN6 centromere fused to an
                     autonomously replicating sequence"
     promoter        2542..2810
                     /label=SNR52 promoter
                     /note="promoter for the S. cerevisiae small nucleolar RNA
                     gene SNR52"
     misc_RNA        2819..2893
                     /label=gRNA scaffold
                     /note="guide RNA scaffold for the Streptococcus pyogenes 
                     CRISPR/Cas9 system"
     terminator      2898..2917
                     /label=SUP4 terminator
                     /note="transcription terminator for the S. cerevisiae SUP4
                     tRNA gene"
     terminator      2969..3158
                     /label=CYC1 terminator
                     /note="transcription terminator for CYC1"
     misc_feature    3377..3394
                     /note="I-SceI; cleavage site"
     misc_feature    3395..3444
                     /label=homology region D0*
                     /note="homology region D0*"
     CDS             3453..7628
                     /label=LYS2
                     /note="alpha-aminoadipate reductase, required for lysine 
                     biosynthesis"
     misc_feature    7836..7885
                     /label=homology region E0*
                     /note="homology region E0*"
     misc_feature    7886..7903
                     /note="I-SceI; cleavage site"

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