pMS2M-PH-gagpol-D64V vector (V017074)

Price Information

Cat No. Plasmid Name Availability Add to cart
V017074 pMS2M-PH-gagpol-D64V 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:
pMS2M-PH-gagpol-D64V
Antibiotic Resistance:
Ampicillin
Length:
10711 bp
Type:
Protein expression
Replication origin:
ori
Host:
Mammalian cells
Growth Strain(s):
Stbl3
Growth Temperature:
37℃

pMS2M-PH-gagpol-D64V vector Map

pMS2M-PH-gagpol-D64V10711 bp5001000150020002500300035004000450050005500600065007000750080008500900095001000010500CMV enhancerCMV promoterMS2-N55KMCSHIV-1 polSP6 promoterbGH poly(A) signalf1 oriSV40 promoterNeoR/KanRSV40 poly(A) signallac promoterCAP binding siteoriAmpRAmpR 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.

pMS2M-PH-gagpol-D64V vector Sequence

LOCUS       V017074                10711 bp    DNA     circular SYN 01-JAN-1980
DEFINITION  Exported.
ACCESSION   V017074
VERSION     V017074
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 10711)
  AUTHORS   .
  TITLE     Direct Submission
FEATURES             Location/Qualifiers
     source          1..10711
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     enhancer        235..614
                     /label="CMV enhancer"
                     /note="human cytomegalovirus immediate early enhancer"
     promoter        615..818
                     /label="CMV promoter"
                     /note="human cytomegalovirus (CMV) immediate early
                     promoter"
     CDS             866..1252
                     /label="MS2-N55K"
                     /note="bacteriophage MS2 coat protein"
     misc_feature    1277..1342
                     /label="MCS"
                     /note="multiple cloning site"
     CDS             1886..3421
                     /gene="gag"
                     /label="Gag polyprotein"
                     /note="Gag polyprotein from Human immunodeficiency virus
                     type 1 group M subtype B (isolate BH10). Accession#:
                     P03347"
     CDS             3265..6225
                     /label="HIV-1 pol"
                     /note="pol protein from human immunodeficiency virus 1"
     promoter        complement(6265..6283)
                     /label="SP6 promoter"
                     /note="promoter for bacteriophage SP6 RNA polymerase"
     polyA_signal    6309..6533
                     /label="bGH poly(A) signal"
                     /note="bovine growth hormone polyadenylation signal"
     rep_origin      6579..7006
                     /label="f1 ori"
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     promoter        7020..7349
                     /label="SV40 promoter"
                     /note="SV40 enhancer and early promoter"
     CDS             7416..8207
                     /label="NeoR/KanR"
                     /note="aminoglycoside phosphotransferase"
     polyA_signal    8384..8517
                     /label="SV40 poly(A) signal"
                     /note="SV40 polyadenylation signal"
     promoter        complement(8602..8632)
                     /label="lac promoter"
                     /note="promoter for the E. coli lac operon"
     protein_bind    complement(8647..8668)
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     rep_origin      complement(8956..9544)
                     /direction=LEFT
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     CDS             complement(9718..10575)
                     /label="AmpR"
                     /note="beta-lactamase"
     promoter        complement(10576..10680)
                     /label="AmpR promoter"