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Pirplus competent cells

For transforming pSM2 vectors
PirPluschemically competent E.coli DH10βpir116  and DH10βF'DOT  were developed for use in rapidly transforming  shRNAmir containing pSM2 vectors.

The shRNAmir  plasmids use the pir -dependent R6Kγ replication origin. The PirPlus E. coli express the π protein (pir gene product), which is essential for cloning, and propagation of the shRNAmir vectors. Additionally the PirPlus strains contain the pir -116 modification allowing for high copy propagation of up to 250 copies per cell compared to wild type pir+ cells1.
 

Benefits of PirPlus™ competent cells:

  • Pir-116 to allow for replication of plasmids containing the R6Kγ origin of replication.
  • aliquot of 100µl are supplied with pUC19 to allow for rapid and easy transformations without wasted reactions.
  • PirPluschemically competent E.coli DH10βpir116 and DH10βF'DOT yield >1 x 107 CFU/µg pUC19.
  • PirPlus DH10βF'DOT is restriction minus mcrA D (mrr-hsdRMS-mcrBC), for cloning of methylated DNA
  • PirPlus DH10βF'DOT contains a tonA mutation conferring resistance to T1 and T5 phages.
  • PirPlus DH10βF'DOT is MAGIC competent for use with mating assisted or MAGIC cloning2

Strains and genotypes:

DH10βpir116: DH10 b UmcC::pir116-Frt

DH10βF'DOT (donor host strain) mcrA Δ (mrr-hsdRMS-mcrBC) Φ 80lacZ Δ M15 Δ lacX74 deoR recA1 endA1 ara Δ 139 Δ (ara,leu)7697 galU galK λ - rpsL nupG λ - tonA umuC::pir116-frtF'(lac + pro +Δ oriT::Tc)

Kit Components: PirPluschemically competent E.coli DH10βpir116 and DH10βF'DOT come complete with:

  • Chemically Competent Cells- 6 x 100µl
  • pUC19 Control Plasmid ( 10pg/µl )- 20µl

Each lot is made using optimized procedures and is tested for efficiency to ensure yields of >1x107 transformants/µg pUC19. The cells are provided in a 100µl aliquot to allow for rapid and easy transformation of your shRNA plasmid. Six aliquots are supplied together with pUC19 control vector.


 

Shipping Information:
Pirplus competent e.coli is shipped on dry ice. Store all components at -80C
References:
  1. Metcalf, W.W. et al. (1994) "Use of the rep technique for allele replacement to construct new Escherichia coli hosts for maintenance of R6K gamma origin plasmids at different copy numbers" Gene 138(1-2):1-7.
     
  2. Li MZ and Elledge S (2005) "MAGIC, an in vivo genetic method for the rapid construction of recombinant DNA molecules" Nat Genet. 2005 Mar;37(3):311-9. Epub 2005 Jan 30
Purchasing Information
Catalog No.
Description
Literature
MBC1249
PirPlus DH10bF\'DOT chemically competent cells
 
MBC3995
PirPlus DH10bpir116 chemically competent cells
 

 

For more information :: Bioxys and Gentaur BVBA :: Av. de l'Armée 68 B4 :: BE-1040 BELGIUM

Email: info@gentaur.com
 

International 

+32 (0) 16 58 90 45

+32 (0) 16 50 90 45

France

01 43 25 01 50

01 43 25 01 60

Italy

02 36 00 65 93

02 36 00 65 94

Germany

0241 6085 13140

0241 6085 33033

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Copyright © 2005 Gentaur BVBA
Last modified: feb-07