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. 2006 May;168(5):1631–1641. doi: 10.2353/ajpath.2006.050521

Figure 2.

Figure 2

Activation status and subcellular localization of Brk in selected T- and B-cell populations. A: Kinase activity assay to determine activation status of Brk as detected by its autophosphorylation and Western blot to examine protein phosphorylation using anti-phosphotyrosine antibody (4G10). The protein phosphorylation is shown also schematically by depicting densitometric analysis data. B: Western blot: Brk protein expression in fractionated nuclei and cytoplasm with A/C lamin (nuclear protein) and a-tubulin (cytoplasmic protein) serving as controls.