pLenti4/TO/V5-DEST vector (V001635)

Price Information

Cat No. Plasmid Name Availability Add to cart
V001635 pLenti4/TO/V5-DEST 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:
pLenti4/TO/V5-DEST
Antibiotic Resistance:
Ampicillin
Length:
8598 bp
Type:
Lentiviral vectors
Replication origin:
ori
Selection Marker:
Zeocin
Promoter:
RSV
Fusion Tag:
V5

pLenti4/TO/V5-DEST vector Map

pLenti4/TO/V5-DEST8598 bp4008001200160020002400280032003600400044004800520056006000640068007200760080008400RSV promoter5' LTR (truncated)HIV-1 PsiRREgp41 peptideProtein TatCMV enhancerCMV promotertet operatortet operatorattR1lac UV5 promoterCmRccdBattR2V5 tagSV40 promoterEM7 promoterBleoR3' LTR (Delta-U3)SV40 poly(A) signalSV40 oriT7 promoterM13 fwdf1 oriAmpR promoterAmpRoriCAP binding sitelac promoterlac operatorM13 revT3 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.

pLenti4/TO/V5-DEST vector Sequence

LOCUS       V001635                 8598 bp    DNA     circular SYN 13-JAN-2022
DEFINITION  Exported.
ACCESSION   V001635
VERSION     V001635
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
            .
REFERENCE   1  (bases 1 to 8598)
  TITLE     Direct Submission
REFERENCE   2  (bases 1 to 8598)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..8598
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     promoter        3..229
                     /label="RSV promoter"
                     /note="Rous sarcoma virus enhancer/promoter"
     LTR             230..410
                     /label="5' LTR (truncated)"
                     /note="truncated 5' long terminal repeat (LTR) from HIV-1"
     misc_feature    457..582
                     /label="HIV-1 Psi"
                     /note="packaging signal of human immunodeficiency virus
                     type 1"
     misc_feature    1075..1308
                     /label="RRE"
                     /note="The Rev response element (RRE) of HIV-1 allows for
                     Rev-dependent mRNA export from the nucleus to the
                     cytoplasm."
     CDS             1493..1537
                     /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             1686..1727
                     /note="Protein Tat from Human immunodeficiency virus type 1
                     group M subtype B (isolate WMJ22). Accession#: P12509"
                     /label="Protein Tat"
     enhancer        1816..2119
                     /label="CMV enhancer"
                     /note="human cytomegalovirus immediate early enhancer"
     promoter        2120..2323
                     /label="CMV promoter"
                     /note="human cytomegalovirus (CMV) immediate early
                     promoter"
     protein_bind    2325..2343
                     /label="tet operator"
                     /note="bacterial operator O2 for the tetR and tetA genes"
     protein_bind    2346..2364
                     /gene="tetO"
                     /label="tetracycline repressor TetR binding site"
                     /bound_moiety="tetracycline repressor TetR"
                     /note="tet operator"
                     /note="bacterial operator O2 for the tetR and tetA genes"
     protein_bind    2405..2529
                     /label="attR1"
                     /note="recombination site for the Gateway(R) LR reaction"
     promoter        2554..2584
                     /label="lac UV5 promoter"
                     /note="E. coli lac promoter with an 'up' mutation"
     CDS             2638..3294
                     /label="CmR"
                     /note="chloramphenicol acetyltransferase"
     CDS             3639..3941
                     /label="ccdB"
                     /note="CcdB, a bacterial toxin that poisons DNA gyrase"
     protein_bind    complement(3985..4109)
                     /label="attR2"
                     /note="recombination site for the Gateway(R) LR reaction"
     CDS             4162..4203
                     /label="V5 tag"
                     /note="epitope tag from simian virus 5"
     promoter        4245..4574
                     /label="SV40 promoter"
                     /note="SV40 enhancer and early promoter"
     promoter        4586..4633
                     /label="EM7 promoter"
                     /note="synthetic bacterial promoter"
     CDS             4652..5023
                     /label="BleoR"
                     /note="antibiotic-binding protein"
     LTR             5119..5352
                     /label="3' LTR (Delta-U3)"
                     /note="self-inactivating 3' long terminal repeat (LTR) from
                     HIV-1"
     polyA_signal    5424..5558
                     /label="SV40 poly(A) signal"
                     /note="SV40 polyadenylation signal"
     rep_origin      5585..5720
                     /label="SV40 ori"
                     /note="SV40 origin of replication"
     promoter        complement(5741..5759)
                     /label="T7 promoter"
                     /note="promoter for bacteriophage T7 RNA polymerase"
     primer_bind     complement(5769..5785)
                     /label="M13 fwd"
                     /note="common sequencing primer, one of multiple similar
                     variants"
     rep_origin      5927..6382
                     /label="f1 ori"
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     promoter        6408..6512
                     /label="AmpR promoter"
     CDS             6513..7370
                     /label="AmpR"
                     /note="beta-lactamase"
     rep_origin      7544..8132
                     /label="ori"
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                     replication"
     protein_bind    8420..8441
                     /label="CAP binding site"
                     /note="CAP binding activates transcription in the presence
                     of cAMP."
     promoter        8456..8486
                     /label="lac promoter"
                     /note="promoter for the E. coli lac operon"
     protein_bind    8494..8510
                     /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)."
     primer_bind     8518..8534
                     /label="M13 rev"
                     /note="common sequencing primer, one of multiple similar
                     variants"
     promoter        8555..8573
                     /label="T3 promoter"
                     /note="promoter for bacteriophage T3 RNA polymerase"