Synthetic -Genes
and  Gene Assembly with ACEMBL !



NEW at ATG!
  -   ACEMBL                               (Please Inquire here)


– AUTOMATABLE DNA
- ASSEMBLY SYSTEM   (Manual Download please click here ....

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First assemble your gene clusters in E. coli then shuttle it to the expression system of your choice.

The DONOR-ACEPTOR based Gene Assembly System with High Efficiency and Variability for E. coli.

Multigene Expression in

  • Protein Complexes
  • Gene Clusters
  • Metabolic Pathway Engineering
  • Assembly of Artificial Genomes

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Media:
http://www.embl.org/aboutus/news/press/2009/03may09/index.html
http://www.psi.ch/medien/medien_news.shtml#multiprotein

The easiest way for assembling your functional DNA - CONSTRUCTS

Here we describe in detail ACEMBL, a system for multi-gene expression in
E. coli that can be used with ease in a truly automated, standarized setup.
E. coli is still the dominant work-horse for recombinant expression, for many
good reasons ranging from low-cost to the availability of a multitude of
expression strains, each with its own merit.

ACEMBL applies tandem recombination steps for rapidly assembling many
genes into multigene expression cassettes. These can be poly-cistronic
or multiple expression modules, or a combination of these elements.

DNA sequences of ACEMBL vectors are provided in the Appendix and can be
copied from there for further use. Multi-protein complex expression is at the
fore-front of contemporary biology.

Several systems have been introduced to co-express proteins in a variety of hosts, each with its own merit. Current systems share in common that they rely, to a varying degree, on standard cloning procedures by restriction enzymes and ligases for the integration of expression elements and their arrangement into functional multi-gene expression vectors. These steps are labor intensive, cumbersome and require significant time and effort, as well as considerable molecular biology expertise for their application.
This is refractory to high-throughput, robotics applications and do not provide flexibility for rapid revision of expression experiments with altered components.
However, automation and flexibility, combined with a reasonable experimental timeframe are a top priority in contemporary protein science.

Entwurf Figure SLIC Prozess1

Entwurf Figure Cre-Lox Prozess2

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Proteincomplexes stable expressed with ACEMBL