Basic Vector Information
The pSilencer 4.1-CMV siRNA Expression vectors are linearized with both BamH 1 and Hind III to facilitate directional cloning. They are also purified to remove the digested insert so that it cannot re-ligate with the vector. This greatly increases the percentage of clones bearing the hairpin siRNA template insert after ligation, reducing the time and effort required to screen clones.
- Vector Name:
- pSilencer 4.1-CMV neo
- Antibiotic Resistance:
- Ampicillin
- Length:
- 4944 bp
- Type:
- RNAi
- Replication origin:
- ori
- Source/Author:
- Thermo Fisher Scientific
- Copy Number:
- High copy number
- Promoter:
- CMV
- Cloning Method:
- Enzyme Cut
- Expression Method:
- Transient
pSilencer 4.1-CMV neo vector Map
pSilencer 4.1-CMV neo vector Sequence
LOCUS 40924_40367 4944 bp DNA circular SYN 08-APR-2021 DEFINITION synthetic circular DNA. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 4944) TITLE Direct Submission REFERENCE 2 (bases 1 to 4944) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article" FEATURES Location/Qualifiers source 1..4944 /mol_type="other DNA" /organism="synthetic DNA construct" primer_bind 379..395 /label=M13 fwd /note="common sequencing primer, one of multiple similar variants" promoter complement(536..739) /label=CMV promoter /note="human cytomegalovirus (CMV) immediate early promoter" enhancer complement(740..1043) /label=CMV enhancer /note="human cytomegalovirus immediate early enhancer" promoter complement(1165..1183) /label=T7 promoter /note="promoter for bacteriophage T7 RNA polymerase" promoter complement(1195..1213) /label=SP6 promoter /note="promoter for bacteriophage SP6 RNA polymerase" primer_bind complement(1233..1249) /label=M13 rev /note="common sequencing primer, one of multiple similar variants" protein_bind complement(1257..1273) /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)." promoter complement(1281..1311) /label=lac promoter /note="promoter for the E. coli lac operon" protein_bind complement(1326..1347) /label=CAP binding site /note="CAP binding activates transcription in the presence of cAMP." rep_origin complement(1635..2223) /direction=LEFT /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" CDS complement(2397..3254) /codon_start=1 /label=AmpR /note="beta-lactamase" /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEYS PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW EPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS LIKHW" polyA_signal complement(3272..3405) /label=SV40 poly(A) signal /note="SV40 polyadenylation signal" CDS complement(3584..4375) /codon_start=1 /label=NeoR/KanR /note="aminoglycoside phosphotransferase" /translation="MIEQDGLHAGSPAAWVERLFGYDWAQQTIGCSDAAVFRLSAQGRP VLFVKTDLSGALNELQDEAARLSWLATTGVPCAAVLDVVTEAGRDWLLLGEVPGQDLLS SHLAPAEKVSIMADAMRRLHTLDPATCPFDHQAKHRIERARTRMEAGLVDQDDLDEEHQ GLAPAELFARLKARMPDGEDLVVTHGDACLPNIMVENGRFSGFIDCGRLGVADRYQDIA LATRDIAEELGGEWADRFLVLYGIAAPDSQRIAFYRLLDEFF" promoter complement(4442..4758) /label=SV40 promoter /note="SV40 enhancer and early promoter"
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