Interaction in vitro; bait produced as a recombinant fusion protein in bacterial system; prey derived from transfected S2 cell extract.
Four clones corresponding to CG2950 were identified.
Positive control.
Source was cell extract of S2 cell line; bait produced from transfected construct; prey produced from endogenous gene.
This interaction persists in the presence of RNaseA.
This interaction persists in the presence of RNaseA.
Source was adult female ovary of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
This interaction persists in the presence of RNaseA.
Source was adult female ovary of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was adult female ovary of transgenic fly line; bait produced from tagged transgenic construct; prey produced from endogenous gene.
This interaction persists in the presence of RNaseA.
Four clones corresponding to CG2950 were identified.
Interaction in vitro; bait produced as a recombinant fusion protein in bacterial system; prey produced as transgenic fusion protein (prey from embryo cDNA expression library).
Two-hybrid system: yeast GAL4-BD/GAL4-AD
Source was yeast cell line; bait produced as transgenic fusion protein; prey produced as transgenic fusion protein (prey was previously cloned reagent).
This interaction persists in the presence of RNaseA.
Source was cell extract of S2 cell line; bait produced from transfected construct; prey produced from endogenous gene.
Source was S2 cell line; bait produced from transfected construct; prey produced from transfected construct.
Interaction in vitro; bait produced as a recombinant fusion protein in bacterial system; prey derived from S2 cells.
Interaction in vitro; bait produced as a recombinant fusion protein in bacterial system; prey derived recombinant fusion protein in bacterial system.