Price Information
| Cat No. | Plasmid Name | Availability | Add to cart |
|---|---|---|---|
| V014674 | pV1081 | 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:
- pV1081
- Antibiotic Resistance:
- Ampicillin
- Length:
- 14621 bp
- Type:
- Genome editing
- Replication origin:
- ori
- Host:
- Yeast
- Selection Marker:
- NAT
- Growth Temperature:
- 37℃
pV1081 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.
pV1081 vector Sequence
LOCUS V014674 14621 bp DNA circular SYN 01-JAN-1980
DEFINITION Exported.
ACCESSION V014674
VERSION V014674
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 14621)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..14621
/mol_type="other DNA"
/organism="synthetic DNA construct"
promoter 622..640
/label="T7 promoter"
/note="promoter for bacteriophage T7 RNA polymerase"
CDS 2667..6770
/label="Cas9"
/note="Cas9 (Csn1) endonuclease from the Streptococcus
pyogenes Type II CRISPR/Cas system"
CDS 6807..6827
/label="SV40 NLS"
/note="nuclear localization signal of SV40 (simian virus
40) large T antigen"
CDS 6831..6851
/label="SV40 NLS"
/note="nuclear localization signal of SV40 (simian virus
40) large T antigen"
CDS 6852..6917
/label="3xFLAG"
/note="three tandem FLAG(R) epitope tags, followed by an
enterokinase cleavage site"
terminator 6982..7229
/label="CYC1 terminator"
/note="transcription terminator for CYC1"
misc_RNA 10155..10230
/label="gRNA scaffold"
/note="guide RNA scaffold for the Streptococcus pyogenes
CRISPR/Cas9 system"
CDS complement(10610..11992)
/gene="BNA5"
/label="Kynureninase"
/note="Kynureninase from Candida albicans (strain SC5314 /
ATCC MYA-2876). Accession#: Q59QC4"
promoter complement(12429..12447)
/label="T3 promoter"
/note="promoter for bacteriophage T3 RNA polymerase"
promoter complement(12516..12546)
/label="lac promoter"
/note="promoter for the E. coli lac operon"
protein_bind complement(12561..12582)
/label="CAP binding site"
/note="CAP binding activates transcription in the presence
of cAMP."
rep_origin complement(12870..13458)
/direction=LEFT
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
CDS complement(13632..14489)
/label="AmpR"
/note="beta-lactamase"
promoter complement(14490..14594)
/label="AmpR promoter"
rep_origin complement(join(14620..14621,1..454))
/direction=LEFT
/label="f1 ori"
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"