C3019I,  NEB 10-beta Competent E. coli (High Efficiency) - 24 transformation reactions (6 tubes)

C3019I, NEB 10-beta Competent E. coli (High Efficiency) - 24 transformation reactions (6 tubes)

C3026J,  SHuffle T7 Competent E. coli - 12 transformation rxns

C3026J, SHuffle T7 Competent E. coli - 12 transformation rxns

C3020K, NEB 10-beta Electrocompetent E. coli - 6 tubes

1.636,25 RON

NEB 10-beta electrocompetent E. coli cells are optimized for high efficiency transformation by electroporation. These cells are ideal for DNA library constructions and all cloning purposes.

SKU
NEB_C3020K

NEB 10-beta electrocompetent E. coli cells are optimized for high efficiency transformation by electroporation. These cells are ideal for DNA library constructions and all cloning purposes.

Highlights

  • DH10B™ derivative
  • Accomodation of large plasmids including BAC and cosmid constructs
  • Efficient transformation of methylated DNA derived from eukaryotic sources and unmethylated DNA derived from PCR, cDNA and other sources
  • Activity of nonspecific endonuclease I eliminated for highest quality plasmid preparations (endA1)
  • Suitable for blue/white screening by α-complementation of the β-galactosidase gene (Φ80ΔlacZM15)
  • Reduced recombination of cloned DNA (recA)
  • Resistance to phage T1 (fhuA)
  • K-12 Strain
  • Free of animal products

Transformation Efficiency

> 2 x 1010 cfu/μg pUC19

Genotype

Δ(ara-leu) 7697 araD139  fhuA ΔlacX74 galK16 galE15 e14-  Φ80dlacZΔM15  recA1 relA1 endA1 nupG  rpsL (StrR) rph spoT1 Δ(mrr-hsdRMS-mcrBC) 

 

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Price 1.375,00 RON (preturile sunt fara TVA)
Description

NEB 10-beta electrocompetent E. coli cells are optimized for high efficiency transformation by electroporation. These cells are ideal for DNA library constructions and all cloning purposes.

Highlights

  • DH10B™ derivative
  • Accomodation of large plasmids including BAC and cosmid constructs
  • Efficient transformation of methylated DNA derived from eukaryotic sources and unmethylated DNA derived from PCR, cDNA and other sources
  • Activity of nonspecific endonuclease I eliminated for highest quality plasmid preparations (endA1)
  • Suitable for blue/white screening by α-complementation of the β-galactosidase gene (Φ80ΔlacZM15)
  • Reduced recombination of cloned DNA (recA)
  • Resistance to phage T1 (fhuA)
  • K-12 Strain
  • Free of animal products

Transformation Efficiency

> 2 x 1010 cfu/μg pUC19

Genotype

Δ(ara-leu) 7697 araD139  fhuA ΔlacX74 galK16 galE15 e14-  Φ80dlacZΔM15  recA1 relA1 endA1 nupG  rpsL (StrR) rph spoT1 Δ(mrr-hsdRMS-mcrBC)