Cite as: Cold Spring Harb. Protoc.; 2009; doi:10.1101/pdb.prot5315
| Protocol |
Adapted from Imaging in Neuroscience and Development (eds. Yuste and Konnerth). CSHL Press, Cold Spring Harbor, NY, USA, 2005.
INTRODUCTION
Synapse formation and modification involve the successive recruitment of pre- and post-synaptic signaling molecules. The procedure presented here investigates the function of specific synaptic factors in gain- and loss-of-function experiments by measuring protein accumulation at synapses using quantitative immunohistochemistry, confocal microscopy, and image analysis. Although the procedure is described for dissociated cultures of hippocampal neurons, it can be extended to various neuronal cell types in culture.
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