pLV2-TRE3GS-MCS-TetOne-CopGFP-Puro vector (V014892) Gene synthesis in pLV2-TRE3GS-MCS-TetOne-CopGFP-Puro backbone

Price Information

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V014892 pLV2-TRE3GS-MCS-TetOne-CopGFP-Puro In stock, instant shipping

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

Basic Vector Information

Vector Name:
pLV2-TRE3GS-MCS-TetOne-CopGFP-Puro
Antibiotic Resistance:
Ampicillin
Length:
10021 bp
Replication origin:
ori
Promoter:
hPGK
Growth Strain(s):
DH10B

pLV2-TRE3GS-MCS-TetOne-CopGFP-Puro vector Map

pLV2-TRE3GS-MCS-TetOne-CopGFP-Puro10021 bp500100015002000250030003500400045005000550060006500700075008000850090009500100003' LTRHIV-1 PsiRREgp41 peptideProtein TatcPPT/CTSTRE3GS promoterhPGK promoterTet-On(R) 3GSV40 promoterCopGFPT2APuroRWPRE5' LTRlac promoterCAP binding siteoriAmpRAmpR promoterSV40 poly(A) signal

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.

pLV2-TRE3GS-MCS-TetOne-CopGFP-Puro vector Sequence

LOCUS       Exported               10021 bp DNA     circular SYN 28-JUL-2025
DEFINITION  Exported.
ACCESSION   V014892
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 10021)
  TITLE     Direct Submission
REFERENCE   2  (bases 1 to 10021)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..10021
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     LTR             1..634
                     /label=3' LTR
                     /note="3' long terminal repeat (LTR) from HIV-1"
     misc_feature    681..806
                     /label=HIV-1 Psi
                     /note="packaging signal of human immunodeficiency virus
                     type 1"
     misc_feature    1303..1536
                     /label=RRE
                     /note="The Rev response element (RRE) of HIV-1 allows for 
                     Rev-dependent mRNA export from the nucleus to the 
                     cytoplasm."
     CDS             1721..1765
                     /label=gp41 peptide
                     /note="antigenic peptide corresponding to amino acids 655
                     to 669 of the HIV envelope protein gp41 (Lutje Hulsik et 
                     al., 2013)"
     CDS             1914..1955
                     /label=Protein Tat
                     /note="Protein Tat from Human immunodeficiency virus type 1
                     group M subtype B (isolate WMJ22). Accession#: P12509"
     misc_feature    2027..2144
                     /label=cPPT/CTS
                     /note="central polypurine tract and central termination
                     sequence of HIV-1"
     promoter        complement(2528..2895)
                     /label=TRE3GS promoter
                     /note="3rd-generation Tet-responsive promoter that can be 
                     activated by binding of Tet-On(R) 3G, modified to eliminate
                     binding sites for endogenous mammalian transcription 
                     factors"
     promoter        2912..3422
                     /label=hPGK promoter
                     /note="human phosphoglycerate kinase 1 promoter"
     CDS             3441..4184
                     /label=Tet-On(R) 3G
                     /note="modified rtTA protein that binds tightly to
                     promoters containing the tet operator in the presence of 
                     doxycycline"
     promoter        4198..4527
                     /label=SV40 promoter
                     /note="SV40 enhancer and early promoter"
     CDS             4578..5243
                     /label=CopGFP
                     /note="green fluorescent protein 2 from Pontellina plumata,
                     also known as ppluGFP2 (Shagin et al., 2004)"
     CDS             5313..5366
                     /label=T2A
                     /note="2A peptide from Thosea asigna virus capsid protein"
     CDS             5376..5972
                     /label=PuroR
                     /note="puromycin N-acetyltransferase"
     misc_feature    5989..6577
                     /label=WPRE
                     /note="woodchuck hepatitis virus posttranscriptional
                     regulatory element"
     LTR             6784..7417
                     /label=5' LTR
                     /note="5' long terminal repeat (LTR) from HIV-1"
     promoter        complement(7594..7624)
                     /label=lac promoter
                     /note="promoter for the E. coli lac operon"
     protein_bind    complement(7639..7660)
                     /label=CAP binding site
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     rep_origin      complement(7948..8536)
                     /direction=LEFT
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     CDS             complement(8710..9567)
                     /label=AmpR
                     /note="beta-lactamase"
     promoter        complement(9568..9672)
                     /label=AmpR promoter
     polyA_signal    9720..9854
                     /label=SV40 poly(A) signal
                     /note="SV40 polyadenylation signal"