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Recent progress in the freeze-etching technique

Philosophical Transactions of the Royal Society of London Series B, Biological Sciences, 1971
Abstract The freeze-etching technique must be improved if structures at the molecular size level are to be seen. The limitations of the technique are discussed here together with the progress made in alleviating them. The vitrification of living specimens is limited by the fact that very high freezing rates are needed.
H Moor
exaly   +3 more sources

Freeze-etching nomenclature

Science, 1975
N B Gilula, Norton B Gilula, H Moor
exaly   +3 more sources

Freeze Fracture and Freeze Etching

2013
Freeze fracture depends on the property of frozen tissues or cells, when cracked open, to split along the hydrophobic interior of membranes, thus revealing broad panoramas of membrane interior. These large panoramas reveal the three-dimensional contours of membranes making the methods well suited to studying changes in membrane architecture.
Douglas E, Chandler, William P, Sharp
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Complementary freeze‐fracture, freeze‐etch specimens

Journal of Microscopy, 1979
SUMMARYA procedure is described for the preparation and comparison of complementary freeze‐fracture‐freeze‐etch specimens. These complementary replicas reveal the value of etching some specimens even when the cryoprotectant concentration amounts to as much as 25% glycerol and 25% sucrose.
R L, Steere, E F, Erbe
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Freeze-Etching of Bacteria

1972
Publisher Summary The first electron micrographs of bacterial cells were published about 20 years ago. These early studies suggested the presence of definite intracellular structures. Sectioning techniques, originally developed for eucaryotic cells, were gradually modified so that thin sections of bacteria could be obtained. These first thin sections
C C, Remsen, S W, Watson
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Bidirectional shadowing in freeze‐etching

Journal of Microscopy, 1983
SUMMARYBidirectional shadowing in freeze‐etching may be achieved by firing an electron‐beam shadowing source, rotating the specimen stage through a desired angle, and re‐firing the shadowing source. It is demonstrated that portrait shadow‐casting, which permits information to be drawn from much of the specimen region lying within primary shadows, can ...
J H, Willison, R D, Moir
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Preparation of Coenocytes for Freeze-Etching

Stain Technology, 1975
Successful freeze-etching of a coenocyte has been accomplished with glutaraldehyde stabilization followed by infiltration with cryoprotectant. Hyphae of the coenocytic water mold Achlya were stabilized with 5% glutaraldehyde in phosphate buffer.
E A, Ellis, J T, Mullins
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Freeze-Etching Simplified

Proceedings, annual meeting, Electron Microscopy Society of America, 1968
Freeze-etching, as a tool in the preparation of biological specimens for electron microscopy, has seen relatively little use since it was introduced in 1957. The involved procedure, originally described, and, until recently, the cost of special equipment, must certainly have played a part in the failure of freeze-etching to become a commonly used ...
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