1967
DOI: 10.1038/216173a0
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Fixation of Ejaculated Spermatozoa for Electron Microscopy

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Cited by 1,373 publications
(497 citation statements)
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“…Briefly, 5-mdiameter frozen serial sagittal or coronal sections were cut with a cryostat and immediately placed on poly-L-lysine-precoated slides (Sigma, St. Louis, Mo.). After air drying for 24 h, cryostat sections were fixed in cold Zamboni's fixative solution (54) and acetone. An avidin-biotin complex technique was used.…”
Section: Methodsmentioning
confidence: 99%
“…Briefly, 5-mdiameter frozen serial sagittal or coronal sections were cut with a cryostat and immediately placed on poly-L-lysine-precoated slides (Sigma, St. Louis, Mo.). After air drying for 24 h, cryostat sections were fixed in cold Zamboni's fixative solution (54) and acetone. An avidin-biotin complex technique was used.…”
Section: Methodsmentioning
confidence: 99%
“…Salivary glands from 15 insects were transferred to Zamboni's fixative solution (Stefanini et al, 1967) and dehydrated in ethanol series, embedded in glycol metacrylate historesin JB4 (Polyscience) and cut in 5 µm thin slices for analysis under light microscope. Sections were stained with haematoxylin and eosin, or submitted to the following histochemical test: mercurybromophenol blue for total proteins, PAS for neutral polysaccharides and glycoconjugates and Nile blue for acid lipids (Pearse, 1980).…”
Section: Morphologymentioning
confidence: 99%
“…Then the mixture was transfered to the cellulose tubes, and dialyzed against distilled wtaer at 4°C for 24 to 48 hr. The fixatives used were; 1) 10% buffered formalin, 2) Zamboni's solution (19,25), 3) 100% ethanol, 4) 100% xylol, and 5) PBS (control). Before dialysis xylol-treated solution was immersed in ethanol to remove xylol.…”
Section: Methodsmentioning
confidence: 99%