Price Information
Cat No. | Plasmid Name | Availability | Add to cart |
---|---|---|---|
V007423 | pBLO 62.5 | 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:
- pBLO 62.5
- Antibiotic Resistance:
- Ampicillin
- Length:
- 7896 bp
- Type:
- Mammalian Expression, CRISPR
- Replication origin:
- ori
- Selection Marker:
- Puromycin
- Copy Number:
- High Copy
- Promoter:
- CBh
pBLO 62.5 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.
pBLO 62.5 vector Sequence
LOCUS 40924_6701 7896 bp DNA circular SYN 13-MAY-2021 DEFINITION Human expression vector for planctomyces CasX and sgRNA. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 7896) AUTHORS Liu JJ, Orlova N, Oakes BL, Ma E, Spinner HB, Baney KLM, Chuck J, Tan D, Knott GJ, Harrington LB, Al-Shayeb B, Wagner A, Brotzmann J, Staahl BT, Taylor KL, Desmarais J, Nogales E, Doudna JA TITLE CasX enzymes comprise a distinct family of RNA-guided genome editors. JOURNAL Nature. 2019 Feb 4. pii: 10.1038/s41586-019-0908-x. doi: 10.1038/s41586-019-0908-x. PUBMED 30718774 REFERENCE 2 (bases 1 to 7896) TITLE Direct Submission REFERENCE 3 (bases 1 to 7896) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Nature. 2019 Feb 4. pii: 10.1038/s41586-019-0908-x. doi: 10.1038/s41586-019-0908-x." COMMENT SGRef: number: 2; type: "Journal Article" FEATURES Location/Qualifiers source 1..7896 /mol_type="other DNA" /organism="synthetic DNA construct" rep_origin 1..589 /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" promoter 651..891 /label=U6 promoter /note="RNA polymerase III promoter for human U6 snRNA" enhancer 1042..1327 /label=CMV enhancer /note="human cytomegalovirus immediate early enhancer; contains an 18-bp deletion relative to the standard CMV enhancer" promoter 1329..1606 /label=chicken beta-actin promoter intron 1607..1834 /label=hybrid intron /note="hybrid between chicken beta-actin (CBA) and minute virus of mice (MMV) introns (Gray et al., 2011)" regulatory 1846..1855 /label=Kozak sequence /note="vertebrate consensus sequence for strong initiation of translation (Kozak, 1987)" /regulatory_class="other" CDS 1858..1878 /codon_start=1 /label=SV40 NLS /note="nuclear localization signal of SV40 (simian virus 40) large T antigen" /translation="PKKKRKV" CDS 4822..4842 /codon_start=1 /label=SV40 NLS /note="nuclear localization signal of SV40 (simian virus 40) large T antigen" /translation="PKKKRKV" CDS 4843..4890 /codon_start=1 /label=2xFLAG /note="two tandem FLAG(R) epitope tags" /translation="DYKDDDDKDYKDDDDK" CDS 4900..4956 /codon_start=1 /label=P2A /note="2A peptide from porcine teschovirus-1 polyprotein" /translation="ATNFSLLKQAGDVEENPGP" CDS 4957..5550 /codon_start=1 /label=PuroR /note="puromycin N-acetyltransferase" /translation="TEYKPTVRLATRDDVPRAVRTLAAAFADYPATRHTVDPDRHIERV TELQELFLTRVGLDIGKVWVADDGAAVAVWTTPESVEAGAVFAEIGPRMAELSGSRLAA QQQMEGLLAPHRPKEPAWFLATVGVSPDHQGKGLGSAVVLPGVEAAERAGVPAFLETSA PRNLPFYERLGFTVTADVEVPEGPRTWCMTRKPGA" polyA_signal 5593..5800 /label=bGH poly(A) signal /note="bovine growth hormone polyadenylation signal" repeat_region 5809..5949 /label=AAV2 ITR /note="inverted terminal repeat of adeno-associated virus serotype 2" rep_origin 6024..6479 /label=f1 ori /note="f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis" primer_bind complement(6496..6515) /label=pRS-marker /note="pRS vectors, use to sequence yeast selectable marker" primer_bind 6615..6637 /label=pGEX 3' /note="pGEX vectors, reverse primer" primer_bind complement(6675..6693) /label=pBRforEco /note="pBR322 vectors, upsteam of EcoRI site, forward primer" promoter 6761..6865 /label=AmpR promoter CDS 6866..7723 /codon_start=1 /label=AmpR /note="beta-lactamase" /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEYS PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW EPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS LIKHW"