pCDNA3.1-Spike(MERS-CoV)-3×FLAG vector (V013534)

Price Information

Cat No. Plasmid Name Availability Add to cart
V013534 pCDNA3.1-Spike(MERS-CoV)-3×FLAG 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:
pCDNA3.1-Spike(MERS-CoV)-3×FLAG
Antibiotic Resistance:
Ampicillin
Length:
10049 bp
Type:
Protein expression
Replication origin:
ori
Host:
Mammalian cells
Selection Marker:
Neo/G418
Promoter:
CMV
Growth Strain(s):
DH5a
Growth Temperature:
37℃

pCDNA3.1-Spike(MERS-CoV)-3×FLAG vector Vector Map

pCDNA3.1-Spike(MERS-CoV)-3×FLAG10049 bp50010001500200025003000350040004500500055006000650070007500800085009000950010000CMV enhancerCMV promoterT7 promoterSpike glycoproteinFLAGbGH poly(A) signalf1 oriSV40 promoterHygRSV40 poly(A) signallac promoterCAP binding siteoriKanR

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.

pCDNA3.1-Spike(MERS-CoV)-3×FLAG vector Sequence

Copy Sequence

Download GeneBank File(.gb)

LOCUS       V013534                10049 bp    DNA     circular SYN 01-JAN-1980
DEFINITION  Exported.
ACCESSION   V013534
VERSION     V013534
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 10049)
  AUTHORS   .
  TITLE     Direct Submission
FEATURES             Location/Qualifiers
     source          1..10049
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     enhancer        253..632
                     /label="CMV enhancer"
                     /note="human cytomegalovirus immediate early enhancer"
     promoter        633..836
                     /label="CMV promoter"
                     /note="human cytomegalovirus (CMV) immediate early
                     promoter"
     promoter        1386..1404
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"
     CDS             1427..5485
                     /gene="S"
                     /label="Spike glycoprotein"
                     /note="Spike glycoprotein from Middle East respiratory
                     syndrome-related coronavirus (isolate United
                     Kingdom/H123990006/2012). Accession#: K9N5Q8"
     CDS             5501..5524
                     /label="FLAG"
                     /note="FLAG(R) epitope tag, followed by an enterokinase
                     cleavage site"
     polyA_signal    5587..5811
                     /label="bGH poly(A) signal"
                     /note="bovine growth hormone polyadenylation signal"
     rep_origin      5857..6285
                     /label="f1 ori"
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     promoter        6299..6628
                     /label="SV40 promoter"
                     /note="SV40 enhancer and early promoter"
     CDS             6677..7699
                     /label="HygR"
                     /note="aminoglycoside phosphotransferase from E. coli"
     polyA_signal    7832..7965
                     /label="SV40 poly(A) signal"
                     /note="SV40 polyadenylation signal"
     promoter        complement(8050..8080)
                     /label="lac promoter"
                     /note="promoter for the E. coli lac operon"
     protein_bind    complement(8095..8116)
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     rep_origin      complement(8404..8992)
                     /direction=LEFT
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     CDS             complement(9095..9907)
                     /label="KanR"
                     /note="aminoglycoside phosphotransferase"