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Type 1 prion disease, whole mount section of medial temporal lobe and hippocampus, 3F4 immunohistochemical stain.

Last updated on Tuesday, April 28 2009 by gliageek

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Type 1 prion disease, whole mount section of medial temporal lobe and hippocampus, 3F4 immunohistochemical stain.
Heavy, diffuse immunoreactivity throughout the temporal lobe neocortex transitions into absence of staining within the hippocampal formation. This is the classic pattern of immunohistochemical staining seen in typical sporadic Jacob Creutzfeldt disease.



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