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pMac-FC vector (V013012)

Price Information

Cat No. Plasmid Name Availability Add to cart
V013012 pMac-FC 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:
pMac-FC
Antibiotic Resistance:
Ampicillin
Length:
10010 bp
Type:
Protein expression, Antibody expression
Replication origin:
ori
Host:
Mammalian cells
Selection Marker:
Neo/G418
Promoter:
SP6
Growth Strain(s):
DH5a
Growth Temperature:
37℃

pMac-FC vector Map

Copy Sequence View Map
pMac-FC10010 bp50010001500200025003000350040004500500055006000650070007500800085009000950010000CMV intron ASP6 promoterbGH poly(A) signalf1 oriSV40NeoR/KanRSV40 poly(A) signallac promoterCAP binding siteoriAmpRAmpR promoterT7Te terminatorSV40 promoterGlutamine synthetasesmall t intronSV40 NLSSV40 poly(A) signalCMV enhancer

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.

pMac-FC vector Sequence

LOCUS       V013012                10010 bp    DNA     circular SYN 01-JAN-1980
DEFINITION  Exported.
ACCESSION   V013012
VERSION     V013012
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 10010)
  AUTHORS   .
  TITLE     Direct Submission
FEATURES             Location/Qualifiers
     source          1..10010
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     intron          142..968
                     /label="CMV intron A"
                     /note="human cytomegalovirus intron A (Chapman et al.,
                     1991)"
     promoter        complement(1774..1792)
                     /label="SP6 promoter"
                     /note="promoter for bacteriophage SP6 RNA polymerase"
     polyA_signal    1818..2042
                     /label="bGH poly(A) signal"
                     /note="bovine growth hormone polyadenylation signal"
     rep_origin      2088..2516
                     /label="f1 ori"
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     promoter        2521..2864
                     /label="SV40"
                     /note="Simian virus 40 enhancer/early promoter"
     CDS             2926..3717
                     /label="NeoR/KanR"
                     /note="aminoglycoside phosphotransferase"
     polyA_signal    3894..4015
                     /label="SV40 poly(A) signal"
                     /note="SV40 polyadenylation signal"
     promoter        complement(4112..4142)
                     /label="lac promoter"
                     /note="promoter for the E. coli lac operon"
     protein_bind    complement(4157..4178)
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     rep_origin      complement(4466..5054)
                     /direction=LEFT
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     CDS             complement(5228..6085)
                     /label="AmpR"
                     /note="beta-lactamase"
     promoter        complement(6086..6190)
                     /label="AmpR promoter"
     terminator      6359..6386
                     /label="T7Te terminator"
                     /note="phage T7 early transcription terminator"
     promoter        6469..6798
                     /label="SV40 promoter"
                     /note="SV40 enhancer and early promoter"
     CDS             6837..7955
                     /gene="GLUL"
                     /label="Glutamine synthetase"
                     /note="Glutamine synthetase from Acomys cahirinus.
                     Accession#: Q9QY94"
     intron          8090..8155
                     /label="small t intron"
                     /note="SV40 (simian virus 40) small t antigen intron"
     CDS             8285..8305
                     /label="SV40 NLS"
                     /note="nuclear localization signal of SV40 (simian virus
                     40) large T antigen"
     polyA_signal    8730..8864
                     /label="SV40 poly(A) signal"
                     /note="SV40 polyadenylation signal"
     enhancer        9433..9812
                     /label="CMV enhancer"
                     /note="human cytomegalovirus immediate early enhancer"