Abstract:
:A monoclonal antibody that reacts with a mid rod fragment of dystrophin was used to localize this protein in the central nervous system (CNS). Due to a low abundance of dystrophin in the CNS, an immunoperoxidase reaction amplified with a biotin-avidin system was used. All Purkinje cells in normal mice were dystrophin positive while the mdx mouse cerebellum was completely devoid of reaction. Dystrophin staining was present in the soma and dendrites of Purkinje cells but not in their axons. This uniform dystrophin labelling in the normal mouse Purkinje cells indicates that this protein is not only localized in synaptic contact regions of the CNS.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
Huard J,Tremblay JPdoi
10.1016/0304-3940(92)90309-ukeywords:
subject
Has Abstractpub_date
1992-03-16 00:00:00pages
105-8issue
1eissn
0304-3940issn
1872-7972pii
0304-3940(92)90309-Ujournal_volume
137pub_type
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