Price Information
Cat No. | Plasmid Name | Availability | Add to cart |
---|---|---|---|
V017439 | pUDE731 | 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:
- pUDE731
- Antibiotic Resistance:
- Ampicillin
- Length:
- 9693 bp
- Type:
- Gene knockout
- Replication origin:
- ori
- Host:
- Yeast
- Selection Marker:
- URA3
- Promoter:
- TEF1
- Growth Strain(s):
- DH5a
- Growth Temperature:
- 37℃
pUDE731 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.
pUDE731 vector Sequence
LOCUS V017439 9693 bp DNA circular SYN 01-JAN-1980 DEFINITION Exported. ACCESSION V017439 VERSION V017439 KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct . REFERENCE 1 (bases 1 to 9693) AUTHORS . TITLE Direct Submission FEATURES Location/Qualifiers source 1..9693 /mol_type="other DNA" /organism="synthetic DNA construct" rep_origin 127..1109 /label="2u ori" /note="yeast 2u plasmid origin of replication" promoter 1136..1240 /label="AmpR promoter" CDS 1241..2098 /label="AmpR" /note="beta-lactamase" rep_origin 2272..2860 /direction=RIGHT /label="ori" /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" promoter 3157..3556 /label="TEF1 promoter" /note="promoter for EF-1-alpha" CDS 3561..7460 /gene="cas12a" /label="CRISPR-associated endonuclease Cas12a" /note="CRISPR-associated endonuclease Cas12a from Francisella tularensis subsp. novicida (strain U112). Accession#: A0Q7Q2" CDS 7461..7508 /label="nucleoplasmin NLS" /note="bipartite nuclear localization signal from nucleoplasmin" CDS 7515..7595 /label="3xHA" /note="three tandem HA epitope tags" CDS 7659..7685 /label="HA" /note="HA (human influenza hemagglutinin) epitope tag" terminator 7728..7917 /label="CYC1 terminator" /note="transcription terminator for CYC1" protein_bind complement(9570..9603) /label="loxP" /note="Cre-mediated recombination occurs in the 8-bp core sequence (ATGTATGC) (Shaw et al., 2021)."