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Table 1 Strains and plasmids used in this study

From: Development of a dual-expression vector facilitated with selection-free PCR recombination cloning strategy

Strain or plasmid

Description

Reference

Strains

 E. coli DH5α

F- Phi80lacZDeltaM15 Delta(lacZYA-argF) U169 recA1 endA1 hsdR17(rk−, mk +) phoA supE44 thi-1 gyrA96 relA1 tonA

Invitrogen

 E. coli D1210HP

F- recA56 thi-1 leu-6 proA2 hsdS20 (rB-mB-) lacY1 galK2 ara-14 mtl-1 xyl-5 lacIq lacY1 endA rpsL20 (Lambdaxis-kil-cI857)

Merck

Plasmids

 pcDNA 3.1(+)

Vector for high-level expression in mammalian cells

Invitrogen

 pElysM

Highly efficient host-killing vector

Ma et al. (2009)

 pC3.1

Derivative of pcDNA 3.1(+), lacking SV40 origin and neomycin selection gene

This study

 pC3.2

Derivative of pC3.1, containing Lac operator, ribosome biding site (RBS), Kozak sequence and 6His tag

This study

 pC3.3

Derivative of pC3.2, containing T7 terminator

This study

 pOmni

Derivative of pC3.3, containing lysis gene E expression cassette

This study

 pIRES2-EGFP

EGFP reporter expression vector

Clontech