Price Information
| Cat No. | Plasmid Name | Availability | Add to cart |
|---|---|---|---|
| V017096 | Cas12f-GE ver4.1 | 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:
- Cas12f-GE ver4.1
- Antibiotic Resistance:
- Ampicillin
- Length:
- 6802 bp
- Type:
- Gene knockout
- Replication origin:
- ori
- Host:
- Mammalian cells
- Promoter:
- CBh
- Growth Strain(s):
- DH5a
- Growth Temperature:
- 37℃
Cas12f-GE ver4.1 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.
Cas12f-GE ver4.1 vector Sequence
LOCUS V017096 6802 bp DNA circular SYN 01-JAN-1980
DEFINITION Exported.
ACCESSION V017096
VERSION V017096
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 6802)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..6802
/mol_type="other DNA"
/organism="synthetic DNA construct"
promoter 6..246
/label="U6 promoter"
/note="RNA polymerase III promoter for human U6 snRNA"
enhancer 545..830
/label="CMV enhancer"
/note="human cytomegalovirus immediate early enhancer;
contains an 18-bp deletion relative to the standard CMV
enhancer"
promoter 832..1106
/label="chicken beta-actin promoter"
CDS 1358..1378
/label="SV40 NLS"
/note="nuclear localization signal of SV40 (simian virus
40) large T antigen"
CDS 1403..2989
/gene="cas12f"
/label="CRISPR-associated endodeoxyribonuclease Cas12f1"
/note="CRISPR-associated endodeoxyribonuclease Cas12f1 from
Uncultured archaeon. Accession#: A0A482D308"
CDS 3107..3820
/label="EGFP"
/note="enhanced GFP"
polyA_signal 3854..4061
/label="bGH poly(A) signal"
/note="bovine growth hormone polyadenylation signal"
repeat_region 4070..4210
/label="AAV2 ITR"
/note="inverted terminal repeat of adeno-associated virus
serotype 2"
rep_origin 4285..4740
/label="f1 ori"
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"
promoter 5022..5126
/label="AmpR promoter"
CDS 5127..5984
/label="AmpR"
/note="beta-lactamase"
rep_origin 6158..6746
/direction=RIGHT
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"