This protocol should find widespread applications for combining analytical methods in

tissue from the same animal, thereby reducing the number of mice required for a given experiment. The structural complexity and heterogeneity of the nervous system requires sophisticated methods for morphological and biochemical analysis, with high selectivity and sensitivity. Immunohistochemistry allows the localisation of proteins (and other tissue constituents) with high spatial resolution; however, it is constrained by the need to protect tissue against degradation by chemical fixation. Aldehydes selleckchem cross-link proteins, thereby immobilizing them in their native subcellular compartments but causing reduced antigenicity due to structural alterations. Biochemical analysis of proteins and nucleic acids typically is performed in extracts prepared from fresh tissue, following decapitation and rapid isolation of the region of interest. Among the methods learn more for protein analysis, Western blotting allows the detection of proteins separated by gel electrophoresis. It lacks spatial resolution, but is highly sensitive and provides a semi-quantitative measure of protein

abundance in samples of interest. It is therefore largely complementary to immunohistochemistry, and often performed with the same antibodies. However, both methods are not readily combined in the same brain due to different requirements for fixation. Isoconazole Numerous experimental paradigms would greatly benefit from concurrent biochemical and immunohistochemical analysis of tissue samples from the same animals (e.g. left and right hemisphere of the brain), requiring a tissue preparation procedure compatible with all analytical methods to be used. While immunohistochemistry can be performed on fresh-frozen tissue (Fritschy et al., 1998), for instance, it is suboptimal for cytoplasmic proteins, which are not immobilised in their native micro-environment and leak out of the cells because freezing

damages the plasma membrane. Post-mortem immersion-fixation of tissue blocks is also suboptimal because of tissue degradation prior to fixation and possible differences in fixation strength between the surface and the depth of the tissue block. Under these conditions, the detection sensitivity of numerous neuronal proteins, notably in pre- and postsynaptic elements, is markedly reduced. We have observed that immunohistochemistry performed in sections prepared from living tissue slices, briefly fixed by immersion in fixative solution, provides excellent detection sensitivity for synaptic proteins, and adequate tissue preservation (Schneider Gasser et al., 2006), but the preparation of these sections is time-consuming and requires considerable experience with histology.