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

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

C3028J,  SHuffle Express Competent E. coli - 12 transformation rxns

C3028J, SHuffle Express Competent E. coli - 12 transformation rxns

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

1.740,97 RON

Chemically competent E. coli K12 cells engineered to form proteins containing disulfide bonds in the cytoplasm. Suitable for T7 promoter driven protein expression.

SKU
NEB_C3026J

Chemically competent E. coli K12 cells engineered to form proteins containing disulfide bonds in the cytoplasm. Suitable for T7 promoter driven protein expression.

Highlights

  • Engineered E. coli K12 to promote disulfide bond formation in the cytoplasm
  • Constitutively expresses a chromosomal copy of the disufide bond isomerase DsbC
  • DsbC promotes the correction of mis-oxidized proteins into their correct form
  • The cytoplasmic DsbC is also a chaperone that can assist in the folding of proteins that do not require disulfide bonds
  • Expresses a chromosomal copy of T7 RNAP
  • Tight control of expression by lacIq allows potentially toxic genes to be cloned
  • Resistance to phage T1 (fhuA2), Nit, Str, Spec

Transformation Efficiency

1 x 106 cfu/µg pUC19 DNA

Genotype

F´ lac, pro, lacIq / Δ(ara-leu)7697 araD139 fhuA2 lacZ::T7 gene1 Δ(phoA)PvuII phoR ahpC* galE (or U) galK λatt::pNEB3-r1-cDsbC (SpecR, lacIq) ΔtrxB rpsL150(StrR) Δgor Δ(malF)3

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Description

Chemically competent E. coli K12 cells engineered to form proteins containing disulfide bonds in the cytoplasm. Suitable for T7 promoter driven protein expression.

Highlights

  • Engineered E. coli K12 to promote disulfide bond formation in the cytoplasm
  • Constitutively expresses a chromosomal copy of the disufide bond isomerase DsbC
  • DsbC promotes the correction of mis-oxidized proteins into their correct form
  • The cytoplasmic DsbC is also a chaperone that can assist in the folding of proteins that do not require disulfide bonds
  • Expresses a chromosomal copy of T7 RNAP
  • Tight control of expression by lacIq allows potentially toxic genes to be cloned
  • Resistance to phage T1 (fhuA2), Nit, Str, Spec

Transformation Efficiency

1 x 106 cfu/µg pUC19 DNA

Genotype

F´ lac, pro, lacIq / Δ(ara-leu)7697 araD139 fhuA2 lacZ::T7 gene1 Δ(phoA)PvuII phoR ahpC* galE (or U) galK λatt::pNEB3-r1-cDsbC (SpecR, lacIq) ΔtrxB rpsL150(StrR) Δgor Δ(malF)3