Skip to main content
. 2021 Sep 13;118(38):e2101592118. doi: 10.1073/pnas.2101592118

Fig. 1.

Fig. 1.

Cellular stress induces TRB3/USP9x-dependent Notch activation in KBP cells. (A) Immunoblot of USP9x, TRB3, MIB1, JAG1, and N1IC in murine KBP cells transfected with either scrambled control (siSCR), TRB3, or USP9x siRNA and treated with either DMSO or 1 μM thapsigargin (Tg). (B) Immunoblot of USP9x, TRB3, MIB1, and N1IC in KBP cells stably expressing a Dox-inducible, shRNA–targeting USP9x, without (−) or with (+) Dox and treated with either DMSO or Tg. (C) Immunoblot of USP9x, TRB3, MIB1, and N1IC in KBP shUSP9x cells cultured in complete (+Leucine) or leucine-deprived (−Leucine) medium without and with Dox. Densitometry of the TRB3 and MIB1 protein bands are presented, relative to β-actin. The expression of β-actin or ERK1/2 are included as loading controls. Molecular weight markers are shown in kilodaltons.