Literature DB >> 13740116

Applications of freeze-substitution to electron microscope studies of invertebrate oocytes.

L I REBHUN.   

Abstract

A modified freeze-substitution process is described which gives a low percentage (less than 5 per cent) of preparations of invertebrate eggs which appear to be ice crystal-free at the resolution of the electron microscope. The mitochondria show no membranes in these preparations but can be recognized by internal spaces with the size and the distribution of the cristae. The Golgi bodies resemble those seen with diffusion fixatives, but the limiting membranes are here double; that is, they appear to be a triple-layered sandwich with two outer dark approximately 25A layers and an inner light layer of the same thickness. The endoplasmic reticulum is clearly present and resembles that seen with diffusion fixatives. Here again, the limiting membranes are double with the same dimensions as those in the Golgi bodies. The membranes of the Golgi bodies and ER are seen after permanganate but not lead hydroxide staining. The hyaloplasm (or "cell sap") is crowded with 150 to 200A particles and these are also seen lining the ER membranes. In general, the structures as seen with the present technique show considerable similarity to those seen with diffusion fixatives.

Entities:  

Keywords:  HISTOLOGICAL TECHNIQUES; OVUM

Mesh:

Substances:

Year:  1961        PMID: 13740116      PMCID: PMC2225041          DOI: 10.1083/jcb.9.4.785

Source DB:  PubMed          Journal:  J Biophys Biochem Cytol        ISSN: 0095-9901


  10 in total

1.  Aster-associated particles in the cleavage of marine invertebrate eggs.

Authors:  L I REBHUN
Journal:  Ann N Y Acad Sci       Date:  1960-10-07       Impact factor: 5.691

2.  Submicroscopic structure of frozen-dried liver specifically stained for electron microscopy. II. Biological.

Authors:  I GERSH; I ISENBERG; W BONDAREFF; J L STEPHENSON
Journal:  Anat Rec       Date:  1957-06

3.  Freeze-solvent substitution technic; a review with an application to fluorescence microscopy.

Authors:  S F PATTEN; K A BROWN
Journal:  Lab Invest       Date:  1958 May-Jun       Impact factor: 5.662

4.  Fixation by freezing-drying for electron microscopy of tissue cells.

Authors:  F S SJOSTRAND; R F BAKER
Journal:  J Ultrastruct Res       Date:  1958-04

5.  Methods and principles of fixation by freeze-substitution.

Authors:  N FEDER; R L SIDMAN
Journal:  J Biophys Biochem Cytol       Date:  1958-09-25

6.  Epoxy resins in electron microscopy.

Authors:  H FINCK
Journal:  J Biophys Biochem Cytol       Date:  1960-02

7.  A device for staining tissue sections for electron microscopy.

Authors:  L D PEACHEY
Journal:  J Biophys Biochem Cytol       Date:  1959-05-25

8.  An electron microscope study of basophile substances of frozen-dried rat liver.

Authors:  H FINCK
Journal:  J Biophys Biochem Cytol       Date:  1958-05-25

9.  Electron microscope and low-angle x-ray diffraction studies of the nerve myelin sheath.

Authors:  H FERNANDEZ-MORAN; J B FINEAN
Journal:  J Biophys Biochem Cytol       Date:  1957-09-25

10.  Staining of tissue sections for electron microscopy with heavy metals. II. Application of solutions containing lead and barium.

Authors:  M L WATSON
Journal:  J Biophys Biochem Cytol       Date:  1958-11-25
  10 in total
  4 in total

1.  SUBMICROSCOPIC CYTOCHEMICAL ORGANIZATION OF INTERPHASE NUCLEI REVEALED BY PROTEIN REAGENTS AND GALLOCYANIN-CHROMALUM. A STUDY OF EHRLICH ASCITES CELLS.

Authors:  B MUNDKUR
Journal:  Z Zellforsch Mikrosk Anat       Date:  1964-06-12

Review 2.  Out with the old and in with the new: rapid specimen preparation procedures for electron microscopy of sectioned biological material.

Authors:  Kent L McDonald
Journal:  Protoplasma       Date:  2013-11-21       Impact factor: 3.356

3.  Frozen thin sections of fresh tissue for electron microscopy, with a description of pancreas and liver.

Authors:  A K Christensen
Journal:  J Cell Biol       Date:  1971-12       Impact factor: 10.539

4.  A simple freeze-fracture replication method for electron microscopy.

Authors:  S Bullivant; A Ames
Journal:  J Cell Biol       Date:  1966-06       Impact factor: 10.539

  4 in total

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