Price Information
| Cat No. | Plasmid Name | Availability | Buy one, get one free! (?) |
|---|---|---|---|
| V015212 | pLJM-SRE-EGFP | In stock, 1 week for quality controls |
Two tubes of lyophilized plasmid will be delivered, each tube is about 5µg.
Basic Vector Information
- Vector Name:
- pLJM-SRE-EGFP
- Antibiotic Resistance:
- Ampicillin
- Length:
- 8037 bp
- Type:
- Transcription factor reporter
- Replication origin:
- ori
- Host:
- Mammalian cells, Lentivirus
- Selection Marker:
- Puro
- Promoter:
- hPGK
- Growth Strain(s):
- Stbl3
- Growth Temperature:
- 37℃
pLJM-SRE-EGFP vector Map
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.
pLJM-SRE-EGFP vector Sequence
LOCUS V015212 8037 bp DNA circular SYN 01-JAN-1980
DEFINITION Exported.
ACCESSION V015212
VERSION V015212
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 8037)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..8037
/mol_type="other DNA"
/organism="synthetic DNA construct"
promoter 256..287
/label="minP"
/note="minimal TATA-box promoter with low basal activity"
CDS 333..1049
/label="EGFP"
/note="enhanced GFP"
misc_feature 1120..1237
/label="cPPT/CTS"
/note="central polypurine tract and central termination
sequence of HIV-1"
promoter 1286..1796
/label="hPGK promoter"
/note="human phosphoglycerate kinase 1 promoter"
CDS 1818..2414
/label="PuroR"
/note="puromycin N-acetyltransferase"
LTR 2545..2778
/label="3' LTR (Delta-U3)"
/note="self-inactivating 3' long terminal repeat (LTR) from
HIV-1"
polyA_signal 2850..2984
/label="SV40 poly(A) signal"
/note="SV40 polyadenylation signal"
rep_origin 3011..3146
/label="SV40 ori"
/note="SV40 origin of replication"
promoter complement(3167..3185)
/label="T7 promoter"
/note="promoter for bacteriophage T7 RNA polymerase"
primer_bind complement(3195..3211)
/label="M13 fwd"
/note="common sequencing primer, one of multiple similar
variants"
rep_origin 3353..3808
/label="f1 ori"
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"
promoter 3834..3938
/label="AmpR promoter"
CDS 3939..4796
/label="AmpR"
/note="beta-lactamase"
rep_origin 4970..5558
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
protein_bind 5846..5867
/label="CAP binding site"
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 5882..5912
/label="lac promoter"
/note="promoter for the E. coli lac operon"
protein_bind 5920..5936
/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 5944..5960
/label="M13 rev"
/note="common sequencing primer, one of multiple similar
variants"
promoter 5981..5999
/label="T3 promoter"
/note="promoter for bacteriophage T3 RNA polymerase"
promoter 6027..6253
/label="RSV promoter"
/note="Rous sarcoma virus enhancer/promoter"
LTR 6254..6434
/label="5' LTR (truncated)"
/note="truncated 5' long terminal repeat (LTR) from HIV-1"
misc_feature 6481..6606
/label="HIV-1 Psi"
/note="packaging signal of human immunodeficiency virus
type 1"
misc_feature 7099..7332
/label="RRE"
/note="The Rev response element (RRE) of HIV-1 allows for
Rev-dependent mRNA export from the nucleus to the
cytoplasm."
CDS 7517..7561
/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 7710..7751
/note="Protein Tat from Human immunodeficiency virus type 1
group M subtype B (isolate WMJ22). Accession#: P12509"
/label="Protein Tat"