Last data update: 26 July 2021 12:16 CEST
Plasmid name: pBC18R (LMBP 9303)
|New search||Print data sheet|
|Price category:||Cat. 1 (cf. price list)|
|Status:||GeneCorner non-core plasmid|
|Depositor's sequence:||not available|
|Promoter:||Phage T7 gene 10 promoter (T7g10)
Escherichia coli lac operon promoter
|Ribosome binding site (RBS) of the Escherichia coli lac Z gene (lacZ)|
|Selection marker:||Ampicillin (amp)|
|Replicon:||Broad-host-range plasmid RK2 origin of transfer (oriT)
Escherichia coli plasmid pMB1 origin
Phage f1 origin
|Host range:||Escherichia coli
Gram-negative bacterial strains
|Parental clone:||pZT18R; pBC19R|
|Further information:||The plasmid was constructed by replacing the 346 bp PvuII fragment containing the MCS of pBC19R with the MCS of pTZ18R.
pBC18R is a mobilisable broad-host-range cloning vector.
Other name of the plasmid is pTZ18R oriTRK2.
|EMBL Accession number:||-|
|Latest sequence update:||03/07/2014|
|Authenticity test:||The plasmid still needs to be subjected to the authenticity test.|
|History of deposit:||This plasmid was deposited by Prof. Dr G. Cornelis(1). It was constructed by Dr B. China(2).
(1) Research Unit in Microorganism Biology, University of Namur, Namur, Belgium
(2) Unit of Microbiology, Catholic University of Louvain, Brussels, Belgium.
|Plasmid reference:||China et al., Mol. Microbiol. 4 (1990), 1585-1593 [PMID: 2287280]
|Restricted distribution:||- BCCM MTA|
|Distributed as:||H/P active culture or plasmid DNA|
|Host for distribution:||Escherichia coli K12 S17-1|
|Related host reference:||Simon et al., Biotechnology 1 (1983), 784-791
|Cultivation medium:||LB-Lennox + ampicillin (100 μg/ml)|
|Other culture collection numbers:||-|
Refer in your Materials and Methods:
|pBC18R (LMBP 9303) is available at BCCM/GeneCorner. This plasmid was deposited by Prof. Dr G. Cornelis and was published in China et al., 1990.|
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.