Last data update: 17 September 2021 10:55 CEST
Plasmid name: pCAGGS-EmCASP-1prop20 (LMBP 4350)
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|Price category:||Cat. 1 (cf. price list)|
|Status:||GeneCorner core plasmid|
(View with Genome Compiler)
Mouse cysteinyl aspartate specific proteinase 1 cDNA (caspase-1, CASP-1, ICE, Casp1); pro-p20 subunit|
|Promoter:||Chicken β-actin/rabbit β-globin hybrid promoter (AG)
Human cytomegalovirus immediate early promoter (CMV-IE); enhancer only
Escherichia coli lac operon promoter
|Terminator:||Rabbit β-globin polyadenylation signal (β-globin polyA)
Simian virus 40 polyadenylation signal (SV40 polyA)
|Selection marker:||Ampicillin (amp)|
|Replicon:||Escherichia coli plasmid pMB1 origin
Simian virus 40 bidirectional origin (SV40)
|Host range:||Escherichia coli
Mammalian cells; SV40 permissive cells
|Parental clone:||pCAGGS-EmCASP-1m3; pCAGGS-EmCASP-1|
|Further information:||The plasmid was constructed as follows: the pro-p20 fragment (from codon 2 up to and including 295) of the mouse cysteinyl aspartate specific proteinase 1 (mCASP-1) wild type cDNA was picked up from pCAGGS-EmCASP-1 by the use of primers and inserted in frame to the N-terminal E-tag between the NotI and XmaI sites of pCAGGS-EmCASP-1m3.
pCAGGS-EmCASP-1prop20 is useful for highly efficient expression of the pro-p20 subunit of mouse caspase-1 under the control of the chicken β-actin/rabbit β-globin hybrid promoter (AG) and the human CMV-IE enhancer in various mammalian cells.
The AG promoter sequence consists of the chicken β-actin promoter, the first exon and part of the first intron (that seems to have a strong enhancer-like activity) linked to a rabbit β-globin fragment, consisting of a 3' part of the second intron (inclusive a branch point which is required for normal splicing reactions) and a 5' part of the third exon.
When cloning a fragment downstream from the lac promoter it may be advisable to use lacI(q) strains in order to prevent fortuitous expression of a possibly noxious polypeptide.
The nucleotide sequence of the mCASP-1 cDNA corresponds with the EMBL Nucleotide Sequence Database accession number BC008152.1.
Other name of the plasmid is pCAGGSEprop20casp-1WT.
|EMBL Accession number:||BC008152.1, view at EMBL, GenBank, DDBJ|
|Latest sequence update:||27/02/2003|
Forward primer (12): 5' CGC.AAG.GAA.GCG.GCC.GCT.GCT.GAC.AAG.ATC.CTG.AGG.GC 3' NotI Reverse primer (13): 5' GT.CGC.CCC.GGG.TTA.TTT.TAA.CAA.CAC.CAC.TCC.TTG.TTT.CTC 3' XmaI Nucleotide sequence at the 5' and 3' end of the mouse CASP-1 pro-p20 cDNA: E-tag --------------------------------------------------- 5' … GAATTCCACC ATG.GGT.GCG.CCG.GTG.CCG.TAT.CCG.GAC.CCG.CTG.GAA.CCG.CGT.GCG.GCC. Met Gly Ala Pro Val Pro Tyr Pro Asp Pro Leu Glu Pro Arg Ala Ala EcoRI BspMII NotI |-> mouse CASP-1 pro p20 p20->| | 2 5 290 295| GCT.GCT.GAC.AAG.ATC.CTG ......... GGA.GTG.GTG.TTG.TTA.AAA.TAA.CCCGGG … 3' Ala Ala Asp Lys Ile Leu Gly Val Val Leu Leu Lys XmaI Punctuation indicates reading frame.
|Authenticity test:||Restriction enzyme pattern analysed at GeneCorner: KpnI, NcoI, SphI and XbaI.|
|History of deposit:||This plasmid was deposited by P. Schotte(1) (2) and Prof. Dr R. Beyaert (1) (2).
(1) Department for Molecular Biomedical Research, VIB, Ghent, Belgium
(2) Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium
|Plasmid reference:||Lamkanfi et al., J. Biol. Chem. 279 (2004), 24785-24793 [PMID: 15039421]
|Restricted distribution:||- BCCM MTA|
|Distributed as:||H/P active culture or plasmid DNA|
|Host for distribution:||Escherichia coli K12 MC1061|
|Host reference:||Casadaban et al., J. Mol. Biol. 138 (1980), 179-207 [PMID: 6997493]
|Related host reference:||Brigé et al., Biochem. J. 394 (2006), 335-344 [PMID: 16293111]
|Cultivation medium:||LB-Lennox + ampicillin (100 μg/ml)|
|Other culture collection numbers:||-|
Refer in your Materials and Methods:
|pCAGGS-EmCASP-1prop20 (LMBP 4350) is available at BCCM/GeneCorner. This plasmid was deposited by P. Schotte and Prof. Dr R. Beyaert and was published in Lamkanfi et al., 2004.|
Note: Up-to-date, validated data are enclosed with the biological material. Nevertheless, these data are a snapshot at a given moment; further updates are always possible.