Abstract
Organ cultured rat diaphragm segments were used to assay a factor which increases endplate-specific acetylcholinesterase. This factor can be substantially purified by vacuum distilling it at 37°C into a dry-ice-acetone cold trap. Sources from which the factor can be distilled include eel electric organ homogenate, rat diaphragm homogenate, and medium conditioned with neurally stimulated muscle.
Original language | English (US) |
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Pages (from-to) | 192-194 |
Number of pages | 3 |
Journal | Brain Research |
Volume | 249 |
Issue number | 1 |
DOIs | |
State | Published - Oct 7 1982 |
Keywords
- acetylcholinesterase
- neuromuscular junction
- organ culture
- rat diaphragm
- trophic factor
ASJC Scopus subject areas
- Neuroscience(all)
- Molecular Biology
- Clinical Neurology
- Developmental Biology