The preparation of cultured cells for X-ray microanalysis.

Scanning microscopy. Supplement Pub Date : 1994-01-01
A Warley
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Abstract

X-ray microanalysis of cells in culture is being used increasingly for the study of relationships between element (ion) content and cell function. There is, however, no one single method which can be used for the preparation of all different cell types for study by microanalysis. Cells in suspension are usually concentrated by centrifugation, before cryofixation, cryosectioning, and freeze drying. On the other hand cells grown as monolayers are more often studied as whole cell mounts, which are washed to remove the external medium before cryofixation and freeze drying. The alternative approach, sectioning of cell monolayers is rarely used. Some of the difficulties encountered in preparing and monolayers of smooth muscle cells for X-ray microanalysis are discussed here.

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用于x射线微量分析的培养细胞的制备。
培养细胞的x射线微分析越来越多地用于研究元素(离子)含量与细胞功能之间的关系。然而,没有一种单一的方法可以用于制备所有不同类型的细胞进行微量分析研究。在冷冻、冷冻切片和冷冻干燥之前,悬浮细胞通常通过离心浓缩。另一方面,作为单层细胞生长的细胞更常作为整个细胞载体进行研究,在冷冻固定和冷冻干燥之前,将其洗涤以去除外部培养基。另一种方法,细胞单层切片很少使用。本文讨论了制备平滑肌细胞和进行x射线微分析时遇到的一些困难。
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Nucleic acid detection by in situ molecular immunogold labeling procedures. Hydration-scanning tunneling microscopy as a reliable method for imaging biological specimens and hydrophilic insulators. Imaging molecular structure of channels and receptors with an atomic force microscope. Atomic force microscopy of DNA, nucleoproteins and cellular complexes: the use of functionalized substrates. Microscopic analysis of DNA and DNA-protein assembly by transmission electron microscopy, scanning tunneling microscopy and scanning force microscopy.
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