pSUMO1 vector (V001155)

Price Information

Cat No. Plasmid Name Availability Add to cart
V001155 pSUMO1 In stock, 1 week for quality controls

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Two tubes of lyophilized plasmid will be delivered, each tube is about 5µg.

Basic Vector Information

Vector Name:
pSUMO1
Antibiotic Resistance:
Streptomycin
Length:
7815 bp
Type:
Bacterial Expression
Replication origin:
CloDF13 ori
Copy Number:
Low Copy
Promoter:
rbs
Cloning Method:
Restriction Enzyme
5' Primer:
GATGAGAAAGAGAATCTCAG
3' Primer:
TGCTAGTTATTGCTCAGCGG

pSUMO1 vector Vector Map

pSUMO17815 bp30060090012001500180021002400270030003300360039004200450048005100540057006000630066006900720075007800T7 promoterlac operatorRBS6xHisSmall ubiquitin-related modifier 1T7 promoterlac operatorSUMO-conjugating enzyme UBC9S-TagT7 terminatorT7 promoterlac operatorSUMO-activating enzyme subunit 2SUMO-activating enzyme subunit 1T7 terminatorSmRAmpR promoterCloDF13 oriCAP binding sitelacIlacI promoter

Plasmid Protocol

1. Centrifuge at 5,000×g for 5 min.

2. Carefully open the tube and add 20 μl of sterile water to dissolve the DNA.

3. Close the tube and incubate for 10 minutes at room temperature.

4. Briefly vortex the tube and then do a quick spin to concentrate the liquid at the bottom. Speed is less than 5000×g.

5. Store the plasmid at -20 ℃.

6. The concentration of plasmid re-measurement sometimes differs from the nominal value, which may be due to the position of the lyophilized plasmid in the tube, the efficiency of the re-dissolution, the measurement bias, and adsorption on the wall of the tube, therefore, it is recommended to transform and extract the plasmid before using it

General Plasmid Transform Protocol

1. Take one 100μl of the competent cells and thaw it on ice for 10min, add 2μl of plasmid, then ice bath for 30min, then heat-shock it at 42℃ for 60s, do not stir, and then ice bath for 2min.

2. Add 900μl of LB liquid medium without antibiotics, and incubate at 37℃ for 45min (30℃ for 1-1.5 hours) with 180rpm shaking.

3. Centrifuge at 6000rpm for 5min, leave only 100μl of supernatant to resuspend the bacterial precipitate and spread it onto the target plasmid-resistant LB plate.

4. Invert the plate and incubate at 37℃ for 14h, or at 30℃ for 20h.

5. Pick a single colony into LB liquid medium, add the corresponding antibiotics, incubate at 220rpm for 14h, and extract the plasmid according to the experimental needs and the instructions of the plasmid extraction kit.

pSUMO1 vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       V001155                 7815 bp    DNA     circular SYN 13-MAY-2021
DEFINITION  Exported.
ACCESSION   V001155
VERSION     V001155
KEYWORDS    pSUMO1
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 7815)
  AUTHORS   Weber AR, Schuermann D, Schar P
  TITLE     Versatile Recombinant SUMOylation System for the Production of
            SUMO-Modified Protein.
  JOURNAL   PLoS One. 2014 Jul 9;9(7):e102157. doi:
            10.1371/journal.pone.0102157. eCollection 2014.
   PUBMED   25007328
REFERENCE   2  (bases 1 to 7815)
  TITLE     Direct Submission
REFERENCE   3  (bases 1 to 7815)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: "PLoS One.";
            date: "2014-07-9"; pages: "
            10.1371/journal.pone.0102157. eCollection 2014"
            SGRef: number: 2; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..7815
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     promoter        2..20
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"
     protein_bind    21..45
                     /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)."
     RBS             60..82
                     /label="RBS"
                     /note="efficient ribosome binding site from bacteriophage
                     T7 gene 10 (Olins and Rangwala, 1989)"
     CDS             101..118
                     /label="6xHis"
                     /note="6xHis affinity tag"
     CDS             140..430
                     /gene="SUMO1"
                     /label="Small ubiquitin-related modifier 1"
                     /note="Small ubiquitin-related modifier 1 from Sus scrofa.
                     Accession#: A7WLH8"
     promoter        579..597
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"
     protein_bind    598..622
                     /label="lac operator"
                     /bound_moiety="lac repressor encoded by lacI"
                     /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)."
     CDS             665..1138
                     /gene="ube2i"
                     /label="SUMO-conjugating enzyme UBC9"
                     /note="SUMO-conjugating enzyme UBC9 from Xenopus
                     tropicalis. Accession#: Q28CQ4"
     CDS             1154..1198
                     /label="S-Tag"
                     /note="affinity and epitope tag derived from pancreatic
                     ribonuclease A"
     terminator      1250..1297
                     /label="T7 terminator"
                     /note="transcription terminator for bacteriophage T7 RNA
                     polymerase"
     promoter        1382..1400
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"
     protein_bind    1401..1425
                     /label="lac operator"
                     /bound_moiety="lac repressor encoded by lacI"
                     /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)."
     CDS             1495..3414
                     /gene="UBA2"
                     /label="SUMO-activating enzyme subunit 2"
                     /note="SUMO-activating enzyme subunit 2 from Homo sapiens.
                     Accession#: Q9UBT2"
     CDS             3446..4483
                     /gene="SAE1"
                     /label="SUMO-activating enzyme subunit 1"
                     /note="SUMO-activating enzyme subunit 1 from Homo sapiens.
                     Accession#: Q9UBE0"
     terminator      4514..4561
                     /label="T7 terminator"
                     /note="transcription terminator for bacteriophage T7 RNA
                     polymerase"
     CDS             complement(4735..5523)
                     /label="SmR"
                     /note="aminoglycoside adenylyltransferase (Murphy, 1985)"
     promoter        complement(5524..5615)
                     /label="AmpR promoter"
     rep_origin      complement(5663..6401)
                     /direction=LEFT
                     /label="CloDF13 ori"
                     /note="Plasmids containing the CloDF13 (CDF) origin of
                     replication can be propagated in E. coli cells that contain
                     additional plasmids with compatible origins."
     protein_bind    complement(6577..6598)
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     CDS             complement(6614..7693)
                     /label="lacI"
                     /note="lac repressor"
     promoter        complement(7694..7771)
                     /label="lacI promoter"