Fig. 2From: Activation of the unfolded protein response and granulovacuolar degeneration are not common features of human prion pathologyImmunohistochemical detection of pIRE1α, pPERK, and CK1δ in AD, vCJD and control brain tissue. Representative pictures are shown of the immunohistochemical detection of pIRE1α (a-d), pPERK (e-h) and CK1δ (i-l) in the hippocampus or frontal cortex of AD, vCJD and non-demented control cases. Immunohistochemical detection of pIRE1α (a), pPERK (e) and CK1δ (i) in neurons in the CA1 region of the hippocampus of a sporadic AD case (case #61). Immunohistochemical detection of pIRE1α (b), pPERK (f) and CK1δ (j) in the frontal cortex of a familial AD case (case #59). Immunohistochemical detection of pIRE1α (c), pPERK (g) and CK1δ (k) in the frontal cortex of a case with vCJD (case #20). Immunohistochemical detection of pIRE1α (d), pPERK (h) and CK1δ (i) in the frontal cortex of a non-demented control case (case #5). The inset (e) shows a typical granular staining which can be referred to as GVD. Immunohistochemical detection is visualized by DAB (brown staining) and nuclei are counterstained with haematoxylin (blue staining). Bar a-l 50 μmBack to article page