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The Nuclear Envelope in Freeze-Etching

The Nuclear Envelope in Freeze-Etching
Author: J. Kartenbeck
Publisher: Springer
Total Pages: 55
Release: 1971-01-01
Genre: Medical
ISBN: 9783540055389

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During the past twenty years the structure of the nuclear envelope, and in particular, that of its most distinct elements, the nuclear pore complexes, has been described from thin section electron microscopy (e,g. , Brettschneider, 1952; Hartmann, 1953; Bahr and Beermann, 1954; Watson, 1954; Kautz and de Marsh, 1955; Watson, 1955), from metal-shadowed (e. g. , Callan and Tomlin, 1950; Gall, 1954, 1956) and negatively stained (e. g. , Franke, 1966, 1967; Gall, 1967; Yoo and Bayley, 1967) preparations of isolated nuclear membranes as revealing characte­ ristics common to euka. ryotic cells in general (recently reviewed, e. g. , in Gouran­ ton, 1969; Stevens and Andre, 1969; Franke, 1970). In the recent years the freeze-etch technique (Steere, 1957) has proved to be a particularly useful tool in studying membraneous structures (e. g. , Moor and Miihlethaler, 1963; Branton and Moor, 1964; Branton, 1966; Koehler, 1968b; Staehelin, l968a; Northcote, 1968a; Branton, 1969; Moor, 1969a). So this method has especially broadened the knowledge, e. g. , on bacterial membranes (Bayer and Remsen, 1970; Nanninga, 1970), on erythrocyte plasma membranes (Weinstein and Bullivant, 1967; Meyer and Winkelmann, 1970; da Silva and Branton, 1970; Tillack and Marchesi, 1970), on liver cell membranes (Chalcroft and Bullivant, 1970), on Golgi membranes (Werz and Kellner, 1970; Staehelin and Kiermayer, 1970), on synaptic vesicles (Moor et al.


The Nuclear Envelope in Freeze-Etching

The Nuclear Envelope in Freeze-Etching
Author: Jurgen Kartenbeck
Publisher: Springer
Total Pages: 60
Release: 2014-01-15
Genre:
ISBN: 9783662103913

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The Nuclear Envelope in Freeze-Etching

The Nuclear Envelope in Freeze-Etching
Author: J. Kartenbeck
Publisher: Springer Science & Business Media
Total Pages: 55
Release: 2013-06-29
Genre: Medical
ISBN: 3662103907

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During the past twenty years the structure of the nuclear envelope, and in particular, that of its most distinct elements, the nuclear pore complexes, has been described from thin section electron microscopy (e, g., Brettschneider, 1952; Hartmann, 1953; Bahr and Beermann, 1954; Watson, 1954; Kautz and de Marsh, 1955; Watson, 1955), from metal-shadowed (e. g., Callan and Tomlin, 1950; Gall, 1954, 1956) and negatively stained (e. g., Franke, 1966, 1967; Gall, 1967; Yoo and Bayley, 1967) preparations of isolated nuclear membranes as revealing characte ristics common to euka. ryotic cells in general (recently reviewed, e. g., in Gouran ton, 1969; Stevens and Andre, 1969; Franke, 1970). In the recent years the freeze-etch technique (Steere, 1957) has proved to be a particularly useful tool in studying membraneous structures (e. g., Moor and Miihlethaler, 1963; Branton and Moor, 1964; Branton, 1966; Koehler, 1968b; Staehelin, l968a; Northcote, 1968a; Branton, 1969; Moor, 1969a). So this method has especially broadened the knowledge, e. g., on bacterial membranes (Bayer and Remsen, 1970; Nanninga, 1970), on erythrocyte plasma membranes (Weinstein and Bullivant, 1967; Meyer and Winkelmann, 1970; da Silva and Branton, 1970; Tillack and Marchesi, 1970), on liver cell membranes (Chalcroft and Bullivant, 1970), on Golgi membranes (Werz and Kellner, 1970; Staehelin and Kiermayer, 1970), on synaptic vesicles (Moor et al.


Freeze-Etch Histology

Freeze-Etch Histology
Author: L. Orci
Publisher: Springer Science & Business Media
Total Pages: 149
Release: 2012-12-06
Genre: Medical
ISBN: 3642660207

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The development of the electron microscope brought one to the other. The purpose of this book is to in a new era, in which cell structures could be provide a bridge, to help those who are familiar visualized down to a macromolecular level. It is of with conventional electron microscopy, to cross course well recognized that some cell components into the less familiar freeze-etching. This has been can be modified or even completely lost during the done by providing paired photographs wherever complex sequence of fixation, dehydration, staining possible, one showing the thin section of a tissue or and plastic embedding which is essential before a a cell, the other a freeze-etch replica of a similar thin section can be obtained. Further, only these cell material. At the same time we have tried to provide components which can be made electron opaque a basis for interpretation of freeze-etched structures, can be visualized. For these reasons, the morpho and we hope the reader will find the first 23 Plates logist and cell biologist alike have to explore alter especially useful in this respect. Because there are native techniques of specimen preparation which many excellent atlases of cell structure available at may avoid some of the artefacts inherent in con the present time, we felt there was no need to ventional thin-section electron microscopy, and at provide lengthy discussions of each plate.


Scanning Electron Microscopy for the Life Sciences

Scanning Electron Microscopy for the Life Sciences
Author: Heide Schatten
Publisher: Cambridge University Press
Total Pages: 275
Release: 2013
Genre: Science
ISBN: 0521195993

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A guide to modern scanning electron microscopy instrumentation, methodology and techniques, highlighting novel applications to cell and molecular biology.


The Cell Nucleus V1

The Cell Nucleus V1
Author: Harris Busch
Publisher: Elsevier
Total Pages: 692
Release: 2012-12-02
Genre: Science
ISBN: 0323143334

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The Cell Nucleus, Volume I reports the basic concepts of cell nucleus, including nuclear structure, the interaction between the nucleus and cytoplasm, and the chromatin. This volume first describes the nucleus’ morphological structures and relates these structures to its functions. It then discusses nuclear organization in plant cells; morphology and biochemistry of the slime mold nucleus; and structure, function, and properties of nuclear envelope. In addition, it addresses the molecular movements between nucleus and cytoplasm against a concentration gradient, presents experiments with animal cell heterokaryons, and explains the genome in specialized cells. It also explores the organization of the chromatin fiber; the human chromosome structure before and after banding; and the ultrastructure and function of heterochromatin and euchromatin.