Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Nuclear extract was treated with DNase and RNase.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Nuclear extract was treated with DNase and RNase.
Source was yeast cell line; bait produced as transgenic fusion protein; prey produced as transgenic fusion protein (prey from embryo cDNA expression library).
Two-hybrid system: yeast LexA-BD/GAL4-AD
Extract was treated with DNase and RNase.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Extract was treated with DNase and RNase.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was embryonic nuclear extract of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Two-hybrid system: yeast LexA-BD/GAL4-AD
Source was yeast cell line; bait produced as transgenic fusion protein; prey produced as transgenic fusion protein (prey from cDNA expression library).
Source was embryonic nuclear extract of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Crude nuclear extract was subjected to several conventional chromatographic steps and gel filtration to purify the 700 kDa TREX-2 complex. This purified fraction was then used for immunoprecipitation.
The interaction was not affected by treatment with DNase or RNase.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Embryonic nuclear extract was treated with DNase and RNase.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Embryonic nuclear extract was treated with DNase and RNase.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was cell extract of S2 cell line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was cell extract of S2 cell line; bait produced from endogenous gene; prey produced from endogenous gene.