C3040H,  NEB Stable Competent E.coli - 20 transformation reactions (20 tubes)

C3040H, NEB Stable Competent E.coli - 20 transformation reactions (20 tubes)

C3019P, NEB 10-beta Competent E. coli (High Efficiency) - 1 x 96 wells (1 plate)

C3019P, NEB 10-beta Competent E. coli (High Efficiency) - 1 x 96 wells (1 plate)

C3040I, NEB Stable Competent E.coli - 24 transformation reactions (6 tubes)

1.871,87 RON

Chemically competent E. coli cells suitable for high efficiency transformation and isolation of plasmid clones containing repeat elements.

SKU
NEB_C3040I

Chemically competent E. coli cells suitable for high efficiency transformation and isolation of plasmid clones containing repeat elements.

Highlights

  • Recommended host strain for cloning genes into retroviral/ lentiviral vectors 
  • Recommended for cloning of direct repeats and inverted repeat sequences
  • Reduced recombination of cloned DNA (recA1)
  • Efficient transformation of methylated DNA derived from eukaryotic sources or unmethylated DNA derived from PCR, cDNA and many other sources [mcrAΔ(mrr-hsdRMS-mcrBC)]
  • Activity of nonspecific endonuclease I (endA1) eliminated for highest quality plasmid preparations
  • Resistance to phage T1 (fhuA)
  • Suitable for blue/white screening with vectors capable of alpha-complementation

Transformation Efficiency

1-3 x 10cfu/µg pUC19 DNA

Genotype

F' proA+B+ lacIq ∆(lacZ)M15 zzf::Tn10 (TetR)/∆(ara-leu) 7697 araD139 fhuA ∆lacX74 galK16 galE15 e14-  Φ80dlacZ∆M15 recA1 relA1 endA1 nupG rpsL (StrR) rph spoT1 ∆(mrr-hsdRMS-mcrBC)

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Price 1.573,00 RON (preturile sunt fara TVA)
Description

Chemically competent E. coli cells suitable for high efficiency transformation and isolation of plasmid clones containing repeat elements.

Highlights

  • Recommended host strain for cloning genes into retroviral/ lentiviral vectors 
  • Recommended for cloning of direct repeats and inverted repeat sequences
  • Reduced recombination of cloned DNA (recA1)
  • Efficient transformation of methylated DNA derived from eukaryotic sources or unmethylated DNA derived from PCR, cDNA and many other sources [mcrAΔ(mrr-hsdRMS-mcrBC)]
  • Activity of nonspecific endonuclease I (endA1) eliminated for highest quality plasmid preparations
  • Resistance to phage T1 (fhuA)
  • Suitable for blue/white screening with vectors capable of alpha-complementation

Transformation Efficiency

1-3 x 10cfu/µg pUC19 DNA

Genotype

F' proA+B+ lacIq ∆(lacZ)M15 zzf::Tn10 (TetR)/∆(ara-leu) 7697 araD139 fhuA ∆lacX74 galK16 galE15 e14-  Φ80dlacZ∆M15 recA1 relA1 endA1 nupG rpsL (StrR) rph spoT1 ∆(mrr-hsdRMS-mcrBC)