BL21 competent cellsToimittaja: Agilent Technologies
AGLS230275EA 229 EURAGLS230275 AGLS230250 AGLS230280 AGLS200131 STRA230240 STRA230134 AGLS235200 AGLS230240 AGLS230255 STRA200131 STRA230265 AGLS200132 STRA230250 AGLS230245 STRA230280 STRA230255 STRA230245 AGLS200133 STRA230275 STRA200132 STRA230130 STRA230132 AGLS230134
BL21 competent cells
BL21 competent cells are an all-purpose strain for high-level protein expression and easy induction.
- High-level protein expression and easy induction
- Can be used with non-T7 RNA polymerase protein expression systems
- Allows the tightest control of protein expression for extremely toxic proteins
- Suitable for expressing proteins from all species, including mammals
- Ideal for difficult protein expression, especially when codon bias is a problem
- Increases transformation efficiency with Hte phenotype
- Derived from Agilent’s high performance BL21-Gold competent cell line
BL21 competent cells are an all-purpose strain for high-level protein expression and easy induction. The basic BL21 strain does not contain the T7 RNA polymerase gene and can be used with non-T7 RNA polymerase protein expression systems. BL21 has the tightest control of protein expression for extremely toxic proteins.
Agilent BL21-CodonPlus competent cells dramatically improve protein expression in E. coli by overcoming codon bias. Codon bias occurs when forced high-level expression of a gene containing codons rarely expressed in E. coli depletes internal tRNA pools. This often results in poor protein synthesis, early termination of the polypeptide chain, or misincorporation of amino acids into the expressed protein. BL21-CodonPlus competent cells are derived from Agilent’s high performance BL21-Gold competent cell line. These cells enable efficient high-level expression of heterologous proteins in Escherichia coli.;Overcoming codon bias saves time and labour by eliminating the need for site-directed mutagenesis or for expressing the protein in a eukaryotic expression system. L21-CodonPlus competent cells are derivatives of BL21-Gold cells that have been engineered to include extra copies of genes that encode tRNAs for these rare E. coli codons. The additional availability of these tRNAs facilitates high level expression of many heterologous recombinant genes in BL21-CodonPlus competent cells. Efficient production of heterologous proteins in E. coli is frequently limited by the rarity of certain tRNAs that are abundant in the organisms from which the heterologous proteins are derived. Forced high-level expression of heterologous proteins can deplete the pool of rare tRNAs and stall translation.
BL21-CodonPlus competent cells also feature the Hte phenotype present in Agilent’s highest efficiency competent cell strain, XL10-Gold. The presence of the Hte phenotype increases the transformation efficiency of the cells. In addition, the gene that encodes endonuclease I (endA), an enzyme that rapidly degrades plasmid DNA isolated by most miniprep procedures, has been inactivated in these cells. These two features enable direct cloning of many protein expression constructs.
BL21-gold competent cells feature the high transformation efficiency phenotype (Hte) and have the gene encoding endonuclease I (endA) inactivated. Together, these two features allow direct cloning for most protein expression constructs. By cloning directly in the strain, you can save two days of work normally spent on subcloning procedures. The DE3-derivatives of BL21 contain the T7 RNA polymerase gene controlled by the lacUV5 promoter. This all-purpose derivative yields high-level expression and provides easy induction. Use this derivative with nontoxic proteins.
Varoitus: For research use only. Not for use in diagnostic procedures.