Price Information
Cat No. | Plasmid Name | Availability | Add to cart |
---|---|---|---|
V000614 | pENTR1A-Huwe1 | 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:
- pENTR1A-Huwe1
- Antibiotic Resistance:
- Kanamycin
- Length:
- 16589 bp
- Type:
- Gateway Entry
- Replication origin:
- ori
- Copy Number:
- Low Copy
- Cloning Method:
- Gateway Cloning
- 5' Primer:
- hHuwe1-R GCCAAATGTTGTAGCCGAGT)(
- 3' Primer:
- hHuwe1-F (TATCAGGACTGCCCACCATT)
pENTR1A-Huwe1 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.
pENTR1A-Huwe1 vector Sequence
LOCUS 40924_17483 16589 bp DNA circular SYN 13-MAY-2021 DEFINITION synthetic circular DNA. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 16589) AUTHORS Cook, Jean TITLE Huwe1 plasmids JOURNAL Unpublished REFERENCE 2 (bases 1 to 16589) TITLE Direct Submission REFERENCE 3 (bases 1 to 16589) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Unpublished" COMMENT SGRef: number: 2; type: "Journal Article" FEATURES Location/Qualifiers source 1..16589 /mol_type="other DNA" /organism="synthetic DNA construct" protein_bind 1..100 /label=attL1 /note="recombination site for the Gateway(R) LR reaction" protein_bind complement(14461..14560) /label=attL2 /note="recombination site for the Gateway(R) LR reaction" CDS 14683..15489 /codon_start=1 /label=KanR /note="aminoglycoside phosphotransferase" /translation="MSHIQRETSRPRLNSNMDADLYGYKWARDNVGQSGATIYRLYGKP DAPELFLKHGKGSVANDVTDEMVRLNWLTEFMPLPTIKHFIRTPDDAWLLTTAIPGKTA FQVLEEYPDSGENIVDALAVSLRRLHSIPVCNCPFNSDRVFRLAQAQSRMNNGLVDASD FDDERNGWPVEQVWKEMHKLLPFSPDSVVTHGDFSLDNLIFDEGKLIGCIDVGRVGIAD RYQDLAILWNCLGEFSPSLQKRLFQKYGIDNPDMNKLQFHLMLDEFF" rep_origin 15582..16170 /direction=RIGHT /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" terminator 16335..16421 /label=rrnB T1 terminator /note="transcription terminator T1 from the E. coli rrnB gene" terminator 16513..16540 /label=rrnB T2 terminator /note="transcription terminator T2 from the E. coli rrnB gene" primer_bind 16548..16571 /label=pENTR-F /note="pENTR vectors, forward primer"