
A rapid and simple method is described for separation of intact synaptosomes, synaptic plasma membranes and vesicles. Two synaptosome fractions were obtained by modified differential centrifugation. The rate zonal zentrifugation in a linear sucrose gradient (very low density) is suitable to obtain fractions highly enriched in synaptic plasma membranes and vesicles. Examination of the prepared fractions was done by enzyme marker activities and electron microscopy
Adenosine Triphosphatases, Synaptic Membranes, Cell Fractionation, Rats, Microscopy, Electron, Centrifugation, Density Gradient, Animals, Magnesium, NADH, NADPH Oxidoreductases, Synaptic Vesicles, Sodium-Potassium-Exchanging ATPase, Synaptosomes
Adenosine Triphosphatases, Synaptic Membranes, Cell Fractionation, Rats, Microscopy, Electron, Centrifugation, Density Gradient, Animals, Magnesium, NADH, NADPH Oxidoreductases, Synaptic Vesicles, Sodium-Potassium-Exchanging ATPase, Synaptosomes
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