Abstract
The Golgi apparatus can be demonstrated in frozen sections of various tissues with an aqueous solution of 1% KMnO4. The externum of Golgi apparatus can be stained with 0.05 gm of benzidine in 10% acetic acid. The internum of Golgi apparatus can be stained with 1 gm of basic fuchsin in 99 ml of 80% ethanol plus 1 ml of HCl. The use of KMnO4 to demonstrate the Golgi apparatus is rapid and reliable as compared to the silver and osmium methods.
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