Price Information
| Cat No. | Plasmid Name | Availability | Add to cart |
|---|---|---|---|
| V016800 | pLenti-Puro-sgAMPKa1 | 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:
- pLenti-Puro-sgAMPKa1
- Antibiotic Resistance:
- Ampicillin
- Length:
- 13013 bp
- Type:
- Gene knockout
- Replication origin:
- ori
- Host:
- Mammalian cells, Lentivirus
- Selection Marker:
- Puro
- Promoter:
- U6
- Growth Strain(s):
- Stbl3
- Growth Temperature:
- 37℃
pLenti-Puro-sgAMPKa1 vector 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.
pLenti-Puro-sgAMPKa1 vector Sequence
LOCUS V016800 13013 bp DNA circular SYN 01-JAN-1980
DEFINITION Exported.
ACCESSION V016800
VERSION V016800
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 13013)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..13013
/mol_type="other DNA"
/organism="synthetic DNA construct"
promoter 1..199
/label="CMV promoter"
/note="human cytomegalovirus (CMV) immediate early
promoter"
misc_feature 444..569
/label="HIV-1 Psi"
/note="packaging signal of human immunodeficiency virus
type 1"
misc_feature 1062..1295
/label="RRE"
/note="The Rev response element (RRE) of HIV-1 allows for
Rev-dependent mRNA export from the nucleus to the
cytoplasm."
CDS 1480..1524
/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 1673..1714
/note="Protein Tat from Human immunodeficiency virus type 1
group M subtype B (isolate WMJ22). Accession#: P12509"
/label="Protein Tat"
misc_feature 1822..1939
/label="cPPT/CTS"
/note="central polypurine tract and central termination
sequence of HIV-1"
promoter 1990..2230
/label="U6 promoter"
/note="RNA polymerase III promoter for human U6 snRNA"
misc_RNA 2260..2335
/label="gRNA scaffold"
/note="guide RNA scaffold for the Streptococcus pyogenes
CRISPR/Cas9 system"
promoter 2397..2608
/label="EF-1-alpha core promoter"
/note="core promoter for human elongation factor
EF-1-alpha"
CDS 2633..6736
/label="Cas9"
/note="Cas9 (Csn1) endonuclease from the Streptococcus
pyogenes Type II CRISPR/Cas system"
CDS 6785..6808
/label="FLAG"
/note="FLAG(R) epitope tag, followed by an enterokinase
cleavage site"
CDS 6818..6874
/label="P2A"
/note="2A peptide from porcine teschovirus-1 polyprotein"
CDS 6875..7468
/label="PuroR"
/note="puromycin N-acetyltransferase"
misc_feature 7487..8075
/label="WPRE"
/note="woodchuck hepatitis virus posttranscriptional
regulatory element"
LTR 8147..8380
/label="3' LTR (Delta-U3)"
/note="self-inactivating 3' long terminal repeat (LTR) from
HIV-1"
polyA_signal 8412..8636
/label="bGH poly(A) signal"
/note="bovine growth hormone polyadenylation signal"
rep_origin 8682..9110
/label="f1 ori"
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"
promoter 9124..9453
/label="SV40 promoter"
/note="SV40 enhancer and early promoter"
promoter 9501..9548
/label="EM7 promoter"
/note="synthetic bacterial promoter"
CDS 9567..9938
/label="BleoR"
/note="antibiotic-binding protein"
promoter 10000..10202
/label="CMV promoter"
/note="human cytomegalovirus (CMV) immediate early
promoter"
promoter complement(10289..10319)
/label="lac promoter"
/note="promoter for the E. coli lac operon"
protein_bind complement(10334..10355)
/label="CAP binding site"
/note="CAP binding activates transcription in the presence
of cAMP."
rep_origin complement(10643..11231)
/direction=LEFT
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
CDS complement(11405..12262)
/label="AmpR"
/note="beta-lactamase"
promoter complement(12263..12367)
/label="AmpR promoter"
enhancer 12633..13012
/label="CMV enhancer"
/note="human cytomegalovirus immediate early enhancer"