Last data update: 26 October 2020 04:25 CET
Plasmid name: pCAGGS-FLAG-hUNRIP (LMBP 5268)
|Price category:||Cat. 1 (cf. price list)|
|Status:||GeneCorner core plasmid|
(View with Genome Compiler)
|Cloned DNA:||Human upstream of N-ras interacting protein cDNA (hUNRIP, hSTRAP)
FLAG epitope tag; N-terminal
|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
|Further information:||The plasmid was constructed as follows: 1) the human upstream of N-ras interacting protein cDNA (hUNRIP, hSTRAP) was amplified by PCR; 2) the SalI/KpnI PCR amplicon was fused to the FLAG epitope tag of the SalI/KpnI opened pCAGGSFLAGmCASP-11m2 plasmid.
pCAGGS-FLAG-hUNRIP is useful for highly efficient expression of hUnrIP 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 this plasmid corresponds with the EMBL Nucleotide Sequence Database accession number LT726996.1.
The nucleotide sequence of the hUNRIP cDNA was obtained from Genbank (Accession number NM_007178.2).
Other name of the plasmid is pCAGGSFLAGUNRIP.
|EMBL Accession number:||NM_007178.2, view at GenBank
LT726996.1, view at EMBL, GenBank, DDBJ
|Latest sequence update:||02/02/2007|
Primers used to amplify the hUNRIP coding sequence: forward: 5' CGGGGTACCATGGCAATGAGACAGACGCCGCTCACC 3' KpnI reverse: 5' TGCGGTCGACTCAGGCCTTAACATCAGGAGCTGAAGG 3' SalI
|Authenticity test:||Restriction enzyme pattern analysed at GeneCorner: DraI, EcoRI, KpnI, NcoI and SalI.|
|History of deposit:||This plasmid was deposited by Y. Bruynooghe(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
|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-FLAG-hUNRIP (LMBP 5268) is available at BCCM/GeneCorner. This plasmid was deposited by Y. Bruynooghe and Prof. Dr R. Beyaert .|
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.