Literature DB >> 6605957

The localization of histochemical and autoradiographic products in the scanning electron microscope by means of atomic number contrast.

I D Bowen, G H Lewis, C Winters.   

Abstract

The role of atomic number contrast and backscattered imaging in the localization of histochemical products and reagents is reviewed. Particular attention is given to the localization of enzymatically released products. A backscattered imaging method is presented which permits the simultaneous demonstration of two label elements in a cryosection examined in the scanning electron microscope. An azo-dye method for the localization of acid phosphatase is combined with an autoradiographic technique for demonstrating [3H]thymidine incorporation. Atomic number contrast, produced by backscattered electrons, permits the detection of a bromine-labelled azo dye, denoting sites of acid phosphatase activity within a cryosection and the simultaneous display of the sites of the silver deposited in an overlying photographic emulsion. The former reveals acid phosphatase to be predominantly associated with thymocyte death and macrophage activity in mouse thymus. The latter pin-points the thymocytes as the main sites of [3H]thymidine incorporation. Atomic number contrast has a useful potential for differentiating between spatially separated histochemical products of differing atomic number in a structural context and also allows a flexible degree of subsurface localization.

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Year:  1983        PMID: 6605957     DOI: 10.1007/bf01002739

Source DB:  PubMed          Journal:  Histochem J        ISSN: 0018-2214


  14 in total

1.  Quantitative evaluation of autoradiographs by X-ray spectroscopy.

Authors:  G M Hodges; M D Muir
Journal:  J Microsc       Date:  1975-07       Impact factor: 1.758

2.  Staining of biological material for the scanning electron microscope.

Authors:  K E Carr; J McGadey
Journal:  J Microsc       Date:  1974-04       Impact factor: 1.758

3.  Scanning-electron-microscope histochemistry using backscatter electrons and metal stains.

Authors:  J L Abraham; P B DeNee
Journal:  Lancet       Date:  1973-05-19       Impact factor: 79.321

4.  The scanning electron microscopic study of the lymph node.

Authors:  S Watanabe
Journal:  Nihon Ketsueki Gakkai Zasshi       Date:  1972-08

5.  The use of x-ray microanalysis to investigate problems encountered in enzyme cytochemistry.

Authors:  T A Ryder; I D Bowen
Journal:  J Microsc       Date:  1974-07       Impact factor: 1.758

6.  Scanning electron microscope histochemistry: the use of backscattered electrons to identify epidermal Langerhans cells in the scanning electron microscope.

Authors:  G M Newcomb; A Boyde
Journal:  Histochem J       Date:  1980-11

7.  Combined autoradiography and histochemistry: the simultaneous detection of 6-3H thymidine and acid phosphatase activity in cryostate sections.

Authors:  G H Lewis; I D Bowen; D Bellamy
Journal:  J Microsc       Date:  1979-11       Impact factor: 1.758

8.  Scanning electron microscopy of hepatic ultrastructure: secondary, backscattered, and transmitted electron imaging.

Authors:  K Miyai; J L Abraham; D S Linthicum; R M Wagner
Journal:  Lab Invest       Date:  1976-10       Impact factor: 5.662

9.  An improved method for combined autoradiography and histochemistry: the simultaneous detection of 6-3H thymidine and acid phosphatase activity in cryostat sections of mouse thymus and duodenum.

Authors:  G H Lewis; I D Bowen
Journal:  J Microsc       Date:  1982-05       Impact factor: 1.758

10.  An X-ray microanalytical azo dye technique for the localization of acid phosphatase activity.

Authors:  I D Bowen; T A Ryder; N L Downing
Journal:  Histochemistry       Date:  1976-10-07
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  1 in total

1.  A methacrylate embedding technique for combined autoradiography and acid phosphatase histochemistry.

Authors:  G H Lewis; I D Bowen
Journal:  Histochem J       Date:  1985-04
  1 in total

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