Competent bacterial cells for chemical or electroporation-based transformation and cloning
Chemically or electroporation-competent bacterial cells for transformation with plasmids, ligation reactions, BAC, or large constructs. The category includes standard cloning strains (DH5-alpha, JM109, TOP10), high-efficiency strains (Stbl3, Stbl4, NEB Stable for unstable repeats), expression strains (BL21(DE3), Rosetta, Lemo21 for difficult proteins), and specialty strains.
Pick by transformation efficiency and end use.
- Efficiency. 10^8 to 10^10 cfu/microgram. Higher for ligation products and large constructs.
- Strain genotype. recA mutations stabilise repeats. endA mutations improve plasmid yield. lacI for IPTG-inducible expression. T7 RNA polymerase for pET expression.
- End application. Cloning, expression, recombineering, library construction each match specific strains.
- Method. Chemical for routine. Electroporation for higher efficiency and large constructs.
- Library construction. For libraries above 10^7 diversity choose electrocompetent with documented efficiency.
Lucigen leads on high-efficiency cloning strains including Stbl3 and Endura for unstable inserts. Antibody Design Labs covers expression and phage display strains.