ProQuest™ Two-Hybrid System with Gateway® Technology
| Reliable Protein-Protein Interaction Results, Fast and Easy. With fewer false positives than other Yeast 2 Hybrid Technologies A key part of gene functional analysis and potential drug target discovery is an understanding of how proteins interact within the cell. The following products facilitate the characterization of these interactions in yeast systems. Using the ProQuest™ Two-Hybrid System with Gateway® Technology provides the ability to quickly and easily move sequences of interest between the ProQuest™ System and other expression and analysis tools using easy recombinational cloning. The ProQuest™ Two-Hybrid System utilizes MaV203 Competent Yeast Cells. A single copy of each of three GAL4 inducible reporter genes (HIS3, URA3, and lacZ) has been integrated into the yeast genome, providing four phenotypes, for easier identification of true interactors. The MaV203 host yeast strain also features low-copy (ARS/CEN) vectors for reduced toxicity and consistent expression levels for more reproducible. By utilizing three reporter genes and low copy number vectors, the ProQuest™ System results in fewer false positives than other systems. A set of five control yeast strains that demonstrate phenotypes for determining the strength of interaction is also provided. |
Bait and Prey
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The ProQuest™ Two Hybrid System with Gateway® Technology provides specially engineered components for bait and prey expression.
The pDEST™ 32 bait vector features:- ARS-CEN sequence for low-copy number maintenance in yeast
- attR sites for Gateway® cloning
- LEU2 for selection of recombinants on medium lacking leucine
pDBleu, the supercoiled parent of pDEST™32 is included with the system to test potential interactors.
The pDEST™22 prey vector features:- ARS-CEN sequence for low-copy number maintenance in yeast
- attR sites for Gateway® cloning
- TRP1 for selection of recombinants on medium lacking tryptophan
pEXP-AD502 for construction of a cDNA or genomic prey is also included with the kit.
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Resources
References
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- Richards MC, Heron SE, Spendlove HE, Scheffer IE, Grinton B, Berkovic SF, Mulley JC, Davy A, Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction. J Med Genet 2004 41(3):e35-e35
- Ueki N, Hayman MJ, Signal-dependent N-CoR requirement for repression by the Ski oncoprotein. J Biol Chem 2003 278(27)24858-24864
- Missero C; Pirro M T; Simeone S; Pischetola M; Di Lauro R; The DNA glycosylase T:G mismatch-specific thymine DNA glycosylase represses thyroid transcription factor-1-activated transcription. J Biol Chem 2001 276(36)33569-75
- Lu Q, Hope LW, Brasch M, Reinhard C, Cohen SN, TSG101 interaction with HRS mediates endosomal trafficking and receptor down-regulation. Proc Natl Acad Sci U S A 2003; 100(13):7626-31



