Price Information
| Cat No. | Plasmid Name | Availability | Add to cart |
|---|---|---|---|
| V013569 | pTD103luxI_sfGFP-BamHI | 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:
- pTD103luxI_sfGFP-BamHI
- Antibiotic Resistance:
- Kanamycin
- Length:
- 5569 bp
- Type:
- Signal transduction
- Replication origin:
- ori
- Host:
- E. coli
- Promoter:
- Luxlp
- Growth Strain(s):
- DH5a
- Growth Temperature:
- 37℃
pTD103luxI_sfGFP-BamHI 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.
pTD103luxI_sfGFP-BamHI vector Sequence
LOCUS V013569 5569 bp DNA circular SYN 01-JAN-1980
DEFINITION Exported.
ACCESSION V013569
VERSION V013569
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
.
REFERENCE 1 (bases 1 to 5569)
AUTHORS .
TITLE Direct Submission
FEATURES Location/Qualifiers
source 1..5569
/mol_type="other DNA"
/organism="synthetic DNA construct"
CDS complement(10..759)
/gene="luxR"
/label="Transcriptional activator protein LuxR"
/note="Transcriptional activator protein LuxR from
Aliivibrio fischeri. Accession#: P12746"
CDS 992..1705
/label="superfolder GFP"
/note="GFP variant that folds robustly even when fused to
poorly folded proteins (Nager et al., 2011)"
terminator 1780..1866
/label="rrnB T1 terminator"
/note="transcription terminator T1 from the E. coli rrnB
gene"
CDS complement(1904..2653)
/gene="luxR"
/label="Transcriptional activator protein LuxR"
/note="Transcriptional activator protein LuxR from
Aliivibrio fischeri. Accession#: P12746"
CDS 2880..3458
/gene="luxI"
/label="Acyl-homoserine-lactone synthase"
/note="Acyl-homoserine-lactone synthase from Aliivibrio
fischeri. Accession#: P12747"
CDS 3459..3491
/label="ssrA tag"
/note="C-terminal peptide that mediates degradation in
bacteria through the ClpXP and ClpAP proteases (McGinness
et al., 2006)"
terminator complement(3515..3558)
/label="rrnB T1 terminator"
/note="transcription terminator T1 from the E. coli rrnB
gene"
rep_origin complement(3763..4351)
/direction=LEFT
/label="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
terminator complement(4439..4533)
/label="lambda t0 terminator"
/note="transcription terminator from phage lambda"
CDS complement(4567..5358)
/label="NeoR/KanR"
/note="aminoglycoside phosphotransferase"