Nuclear extract was purified through several different chromatographic steps, selecting for nucleosome disruption activity.
Identity of 140 kDa band as Iswi confirmed by both western blot and mass spectrometry.
Source was embryonic nuclear extract of wild-type fly line; proteins produced from endogenous genes.
Nuclear extract was purified through several different chromatographic steps, selecting for nucleosome disruption activity.
Source was embryonic nuclear extract of wild-type fly line; proteins produced from endogenous genes.
Source was cell extract of S2 cell line; bait produced from transfected construct; prey produced from transfected construct.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was cell extract of Sf9 cell line; bait produced from recombinant baculovirus construct; prey produced from recombinant baculovirus construct.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Positive control.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Positive control.
Source was embryos of wild-type fly line; bait produced from endogenous gene; prey produced from endogenous gene.
Source was nuclear extract of S2 cell line; bait produced from endogenous gene; prey produced from endogenous gene.