pETDuet1-Promoter-mcjB-mcjC-mcjD(coli)-T7-msyB-mcjA(coli) vector (V014059)

Price Information

Cat No.	Plasmid Name	Availability	Add to cart
V014059	pETDuet1-Promoter-mcjB-mcjC-mcjD(coli)-T7-msyB-mcjA(coli)	In stock, 1 week for quality controls	Buy one, get one free!

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

Basic Vector Information

Vector Name:: pETDuet1-Promoter-mcjB-mcjC-mcjD(coli)-T7-msyB-mcjA(coli)

Antibiotic Resistance:: Ampicillin

Length:: 9549 bp

Type:: Protein expression

Replication origin:: ori

Host:: E. coli

Promoter:: T7

Growth Strain(s):: DH5a

Growth Temperature:: 37℃

pETDuet1-Promoter-mcjB-mcjC-mcjD(coli)-T7-msyB-mcjA(coli) vector Vector Map

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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.

pETDuet1-Promoter-mcjB-mcjC-mcjD(coli)-T7-msyB-mcjA(coli) vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       V014059                 9549 bp    DNA     circular SYN 01-JAN-1980
DEFINITION  Exported.
ACCESSION   V014059
VERSION     V014059
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 9549)
  AUTHORS   .
  TITLE     Direct Submission
FEATURES             Location/Qualifiers
     source          1..9549
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     CDS             2265..4004
                     /gene="mcjD"
                     /label="Microcin-J25 export ATP-binding/permease protein
                     McjD"
                     /note="Microcin-J25 export ATP-binding/permease protein
                     McjD from Escherichia coli. Accession#: Q9X2W0"
     promoter        4079..4097
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"
     protein_bind    4098..4122
                     /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)."
     CDS             4537..4707
                     /gene="mcjA"
                     /label="Microcin J25"
                     /note="Microcin J25 from Escherichia coli. Accession#:
                     Q9X2V7"
     CDS             4723..4767
                     /label="S-Tag"
                     /note="affinity and epitope tag derived from pancreatic
                     ribonuclease A"
     terminator      4819..4866
                     /label="T7 terminator"
                     /note="transcription terminator for bacteriophage T7 RNA
                     polymerase"
     rep_origin      4903..5358
                     /label="f1 ori"
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     CDS             complement(5476..6333)
                     /label="AmpR"
                     /note="beta-lactamase"
     promoter        complement(6334..6426)
                     /label="AmpR promoter"
     rep_origin      6507..7095
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     misc_feature    complement(7281..7423)
                     /label="bom"
                     /note="basis of mobility region from pBR322"
     CDS             complement(7528..7716)
                     /label="rop"
                     /note="Rop protein, which maintains plasmids at low copy
                     number"
     protein_bind    complement(8254..8275)
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     CDS             complement(8291..9370)
                     /label="lacI"
                     /note="lac repressor"
     promoter        complement(9371..9448)
                     /label="lacI promoter"