pGGC001 vector (V006017)

Basic Vector Information

Vector Name:
pGGC001
Antibiotic Resistance:
Ampicillin
Length:
3564 bp
Type:
Cloning vector
Replication origin:
ori
Source/Author:
Lampropoulos A, Sutikovic Z, Wenzl C, Maegele I, Lohmann JU, Forner J.
Promoter:
SP6

pGGC001 vector Vector Map

pGGC0013564 bp6001200180024003000AmpR promoterAmpRoriCAP binding sitelac promoterlac operatorSP6 promoterBsaI recognition siteProtein WUSCHELBsaI recognition siteT7 promoter

pGGC001 vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       V006017                 3564 bp    DNA     circular SYN 18-DEC-2018
DEFINITION  Exported.
ACCESSION   V006017
VERSION     V006017
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 3564)
  AUTHORS   Lampropoulos A, Sutikovic Z, Wenzl C, Maegele I, Lohmann JU, Forner
            J.
  TITLE     GreenGate - A Novel, Versatile, and Efficient Cloning System for
            Plant Transgenesis
  JOURNAL   PLoS ONE 8 (12), E83043 (2013)
   PUBMED   24376629
REFERENCE   2  (bases 1 to 3564)
  AUTHORS   Forner J.
  TITLE     Direct Submission
  JOURNAL   Submitted (28-SEP-2013) Centre for Organismal Studies,
            Ruprecht-Karls-Universitaet Heidelberg, Im Neuenheimer Feld 230,
            Heidelberg D-69221, Germany
REFERENCE   3  (bases 1 to 3564)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 3564)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     ##Assembly-Data-START##
            Sequencing Technology :: Sanger dideoxy sequencing
            ##Assembly-Data-END##
            SGRef: number: 1; type: "Journal Article"; journalName: "PLoS ONE";
            date: "2013"; volume: "8"; issue: "12"; pages: "E83043"
            SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
            (28-SEP-2013) Centre for Organismal Studies,
            Ruprecht-Karls-Universitaet Heidelberg, Im Neuenheimer Feld 230,
            Heidelberg D-69221, Germany"
            SGRef: number: 3; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..3564
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     promoter        96..200
                     /label="AmpR promoter"
     CDS             201..1058
                     /label="AmpR"
                     /note="beta-lactamase"
     rep_origin      1232..1820
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     protein_bind    2108..2129
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     promoter        2144..2174
                     /label="lac promoter"
                     /note="promoter for the E. coli lac operon"
     protein_bind    2182..2198
                     /label="lac operator"
                     /note="The lac repressor binds to the lac operator to
                     inhibit transcription in E. coli. This inhibition can be
                     relieved by adding lactose or
                     isopropyl-beta-D-thiogalactopyranoside (IPTG)."
     promoter        2212..2230
                     /label="SP6 promoter"
                     /note="promoter for bacteriophage SP6 RNA polymerase"
     misc_feature    2241..2246
                     /label="BsaI recognition site"
                     /note="BsaI recognition site"
     CDS             2254..3129
                     /gene="WUS"
                     /label="Protein WUSCHEL"
                     /note="Protein WUSCHEL from Arabidopsis thaliana.
                     Accession#: Q9SB92"
     misc_feature    complement(3135..3140)
                     /label="BsaI recognition site"
                     /note="BsaI recognition site"
     promoter        complement(3151..3169)
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"

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