Price Information
Cat No. | Plasmid Name | Availability | Add to cart |
---|---|---|---|
V013683 | pLKO.1-mCherry-P2A-Neo | 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:
- pLKO.1-mCherry-P2A-Neo
- Antibiotic Resistance:
- Ampicillin
- Length:
- 8015 bp
- Type:
- RNA interference
- Replication origin:
- ori
- Host:
- Mammalian cells, Lentivirus
- Selection Marker:
- Neo/G418
- Promoter:
- hPGK
- Growth Strain(s):
- Stbl3
- Growth Temperature:
- 37℃
pLKO.1-mCherry-P2A-Neo 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.
pLKO.1-mCherry-P2A-Neo vector Sequence
LOCUS V013683 8015 bp DNA circular SYN 01-JAN-1980 DEFINITION Exported. ACCESSION V013683 VERSION V013683 KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct . REFERENCE 1 (bases 1 to 8015) AUTHORS . TITLE Direct Submission FEATURES Location/Qualifiers source 1..8015 /mol_type="other DNA" /organism="synthetic DNA construct" promoter 7..507 /label="hPGK promoter" /note="human phosphoglycerate kinase 1 promoter" CDS 516..1223 /label="mCherry" /note="monomeric derivative of DsRed fluorescent protein (Shaner et al., 2004)" CDS 1299..2090 /label="NeoR/KanR" /note="aminoglycoside phosphotransferase from Tn5" LTR 2221..2454 /label="3' LTR (Delta-U3)" /note="self-inactivating 3' long terminal repeat (LTR) from HIV-1" polyA_signal 2526..2660 /label="SV40 poly(A) signal" /note="SV40 polyadenylation signal" rep_origin 2687..2822 /label="SV40 ori" /note="SV40 origin of replication" promoter complement(2843..2861) /label="T7 promoter" /note="promoter for bacteriophage T7 RNA polymerase" primer_bind complement(2871..2887) /label="M13 fwd" /note="common sequencing primer, one of multiple similar variants" rep_origin 3029..3484 /label="f1 ori" /note="f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis" promoter 3510..3614 /label="AmpR promoter" CDS 3615..4472 /label="AmpR" /note="beta-lactamase" rep_origin 4646..5234 /label="ori" /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" protein_bind 5522..5543 /label="CAP binding site" /note="CAP binding activates transcription in the presence of cAMP." promoter 5558..5588 /label="lac promoter" /note="promoter for the E. coli lac operon" protein_bind 5596..5612 /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 5620..5636 /label="M13 rev" /note="common sequencing primer, one of multiple similar variants" promoter 5657..5675 /label="T3 promoter" /note="promoter for bacteriophage T3 RNA polymerase" promoter 5703..5929 /label="RSV promoter" /note="Rous sarcoma virus enhancer/promoter" LTR 5930..6110 /label="5' LTR (truncated)" /note="truncated 5' long terminal repeat (LTR) from HIV-1" misc_feature 6157..6282 /label="HIV-1 Psi" /note="packaging signal of human immunodeficiency virus type 1" misc_feature 6775..7008 /label="RRE" /note="The Rev response element (RRE) of HIV-1 allows for Rev-dependent mRNA export from the nucleus to the cytoplasm." CDS 7193..7237 /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 7386..7427 /note="Protein Tat from Human immunodeficiency virus type 1 group M subtype B (isolate WMJ22). Accession#: P12509" /label="Protein Tat" promoter 7535..7775 /label="U6 promoter" /note="RNA polymerase III promoter for human U6 snRNA" misc_feature 7846..7963 /label="cPPT/CTS" /note="central polypurine tract and central termination sequence of HIV-1" promoter 8012..8015 /label="hPGK promoter" /note="human phosphoglycerate kinase 1 promoter"