Abstract

The Expresso® Cloning and Expression Systems use Expressioneering™ Technology, an in vivo recombinational cloning strategy, to dramatically increase the speed, efficiency and success of target gene cloning and soluble protein expression in E. coli and mammalian system. Expressioneering allows directional cloning of PCR products into pre‐processed expression vectors without sample clean‐up or enzyme treatment. Expresso System vectors were constructed with various inducible promoters, N‐ or C‐terminal 6xHis tags, and an optional cleavable SUMO tag for improved recombinant protein solubility in bacterial systems.The Expresso T7 System uses an IPTG‐inducible T7‐lac promoter and the Expresso Rhamnose Systems features the tunable, rhamnose‐inducible, rhaPBAD promoter, and uses a single host strain for both cloning and expression.The new Expresso CMV system for mammalian protein production utilizes the same Expressioneering technology to provide rapid, precise, and directional insertion of fragments into the cloning site. The small size of the pME‐HA vector (3.4 kb) and minimal amount of bacterial DNA sequence supports robust protein expression, higher transfection efficiency and simplifies subsequent manipulations. The Expresso CMV vector allows addition of the HA tag for immono‐detection or affinity purification.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.