The ace of the Two-hybrid systems

products | two- & one hybrid systems | Grow´n´Glow ACE1

Two- & One Hybrid Systems

Grow´n´Glow ACE1 Yeast Two Hybrid System

Features and Advantages:

• allows to select for different protein-protein interaction strengths
• more efficient detection of protein interactions in vivo by the copper-inducible CUP1/ACE1 system
• fewer false-positives by stringent selection for copper-resistance
• improved time-saving selection of positives with the well-established advantageous GFP reporter
• no requirement for external substrates such as X-Gal when screening for positives
• suited for the development of high-throughput-screening assays
  

General Product Description:

The yeast two-hybrid system is an intelligent versatile genetic approach for the detection of protein-protein interactions in vivo. It depends on the ability of specific separated DNA binding and transactivation domains to reconstitute an active transcription factor complex if interacting proteins are fused to these domains. Clones expressing interacting proteins are consequently detected through the activity of reporter genes.

MoBiTec´s new ACE1 Two Hybrid System is a powerful tool for gene discovery and functional analysis and very useful for efficiently identifying protein-protein interactions in vivo. It combines the advantages of the copper-inducible transcription factor ACE1 and the copper resistance-mediating CUP1 gene with the proven green fluorescence protein (GFP) as reporter. Interaction of two proteins fused to the DNA-binding and transactivation domains of ACE1, respectively, can be consequently detected by 1) growth of the cells on copper-containing media and 2) the copper-dependent expression of the strongly-fluorescent GFPuv which renders those colonies to fluoresce bright green under UV light.
Thus, this novel innovative technique greatly facilitates an efficient one-step selection of potential positives expressing interacting proteins in copper-containing media and under UV light. It allows a fast, highly sensitive and more reliable monitoring of protein interactions in living cells because interacting clones are identified by a growth selection as well as a strong fluorescence signal. Changing the copper concentration allows to select for different protein-protein interaction strengths.

Downloads: Handbook