Price Information
Cat No. | Plasmid Name | Availability | Add to cart |
---|---|---|---|
V005560 | pHGWA | 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
Vectors p0GWA and pHGWA were constructed by modifying the pET22b vector. By replacing the multiple cloning site with the Gateway cassette, it allows a rapid insertion of fusion encoding sequences.
- Vector Name:
- pHGWA
- Antibiotic Resistance:
- Ampicillin
- Length:
- 7132 bp
- Type:
- Expression vector
- Replication origin:
- ori
- Source/Author:
- Busso D, Delagoutte-Busso B, Moras D.
pHGWA 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.
References
- Busso D, Delagoutte-Busso B, Moras D. Construction of a set Gateway-based destination vectors for high-throughput cloning and expression screening in Escherichia coli. Anal Biochem. 2005;343(2):313-321. doi:10.1016/j.ab.2005.05.015
pHGWA vector Sequence
LOCUS 40924_24543 7132 bp DNA circular SYN 18-DEC-2018 DEFINITION Expression vector pHGWA, complete sequence. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 7132) AUTHORS Busso D, Delagoutte-Busso B, Moras D. TITLE Construction of a set Gateway-based destination vectors for high-throughput cloning and expression screening in Escherichia coli JOURNAL Anal. Biochem. 343 (2), 313-321 (2005) PUBMED 15993367 REFERENCE 2 (bases 1 to 7132) AUTHORS Busso D, Delagoutte-Busso B, Salim L, Moras D. TITLE Direct Submission JOURNAL Submitted (25-APR-2008) Structural Biology and Genomics Platform, IGBMC, 1, rue Laurent Fries, Illkirch 67404, France REFERENCE 3 (bases 1 to 7132) TITLE Direct Submission REFERENCE 4 (bases 1 to 7132) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Anal. Biochem."; date: "2005"; volume: "343"; issue: "2"; pages: "313-321" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (25-APR-2008) Structural Biology and Genomics Platform, IGBMC, 1, rue Laurent Fries, Illkirch 67404, France" COMMENT SGRef: number: 3; type: "Journal Article" FEATURES Location/Qualifiers source 1..7132 /mol_type="other DNA" /organism="synthetic DNA construct" promoter 27..45 /label=T7 promoter /note="promoter for bacteriophage T7 RNA polymerase" protein_bind 46..70 /label=lac operator /note="The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-beta-D-thiogalactopyranoside (IPTG)." RBS 85..107 /label=RBS /note="efficient ribosome binding site from bacteriophage T7 gene 10 (Olins and Rangwala, 1989)" CDS 126..143 /codon_start=1 /label=6xHis /note="6xHis affinity tag" /translation="HHHHHH" protein_bind 162..286 /label=attR1 /note="recombination site for the Gateway(R) LR reaction" promoter 311..341 /label=lac UV5 promoter /note="E. coli lac promoter with an 'up' mutation" CDS 395..1051 /codon_start=1 /label=CmR /note="chloramphenicol acetyltransferase" /translation="MEKKITGYTTVDISQWHRKEHFEAFQSVAQCTYNQTVQLDITAFL KTVKKNKHKFYPAFIHILARLMNAHPEFRMAMKDGELVIWDSVHPCYTVFHEQTETFSS LWSEYHDDFRQFLHIYSQDVACYGENLAYFPKGFIENMFFVSANPWVSFTSFDLNVANM DNFFAPVFTMGKYYTQGDKVLMPLAIQVHHAVCDGFHVGRMLNELQQYCDEWQGGA" CDS 1396..1698 /codon_start=1 /label=ccdB /note="CcdB, a bacterial toxin that poisons DNA gyrase" /translation="MQFKVYTYKRESRYRLFVDVQSDIIDTPGRRMVIPLASARLLSDK VSRELYPVVHIGDESWRMMTTDMASVPVSVIGEEVADLSHRENDIKNAINLMFWGI" protein_bind complement(1742..1866) /label=attR2 /note="recombination site for the Gateway(R) LR reaction" CDS 1880..1897 /codon_start=1 /label=6xHis /note="6xHis affinity tag" /translation="HHHHHH" terminator 1964..2011 /label=T7 terminator /note="transcription terminator for bacteriophage T7 RNA polymerase" rep_origin 2048..2503 /label=f1 ori /note="f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis" promoter 2530..2634 /label=AmpR promoter CDS 2635..3492 /codon_start=1 /label=AmpR /note="beta-lactamase" /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEYS PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW EPELNEAIPNDERDTTMPAAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS LIKHW" rep_origin 3666..4254 /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" misc_feature complement(4440..4582) /label=bom /note="basis of mobility region from pBR322" CDS complement(4687..4875) /codon_start=1 /label=rop /note="Rop protein, which maintains plasmids at low copy number" /translation="VTKQEKTALNMARFIRSQTLTLLEKLNELDADEQADICESLHDHA DELYRSCLARFGDDGENL" protein_bind complement(5650..5671) /label=CAP binding site /note="CAP binding activates transcription in the presence of cAMP." CDS complement(5687..6766) /codon_start=1 /label=lacI /note="lac repressor" /translation="VKPVTLYDVAEYAGVSYQTVSRVVNQASHVSAKTREKVEAAMAEL NYIPNRVAQQLAGKQSLLIGVATSSLALHAPSQIVAAIKSRADQLGASVVVSMVERSGV EACKAAVHNLLAQRVSGLIINYPLDDQDAIAVEAACTNVPALFLDVSDQTPINSIIFSH EDGTRLGVEHLVALGHQQIALLAGPLSSVSARLRLAGWHKYLTRNQIQPIAEREGDWSA MSGFQQTMQMLNEGIVPTAMLVANDQMALGAMRAITESGLRVGADISVVGYDDTEDSSC YIPPLTTIKQDFRLLGQTSVDRLLQLSQGQAVKGNQLLPVSLVKRKTTLAPNTQTASPR ALADSLMQLARQVSRLESGQ" promoter complement(6767..6844) /label=lacI promoter