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1
Identification of glycogen in electron micrographs of thin tissue sections.在薄组织切片的电子显微照片中鉴定糖原。
J Biophys Biochem Cytol. 1960 Dec;8(3):575-89. doi: 10.1083/jcb.8.3.575.
2
The fine structure of endothelium of large arteries.大动脉内皮的精细结构。
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3
Electron microscope observations on the behavior of the bacterial cytoplasmic membrane during cellular division.关于细菌细胞质膜在细胞分裂过程中行为的电子显微镜观察
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A simplified method of staining thin sections of biolgical material with lead hydroxide for electron microscopy.一种用氢氧化铅对生物材料薄片进行染色以用于电子显微镜检查的简化方法。
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5
[Morphology of glycogen. Electron microscopic study of the negative stains of particulate glycogen].[糖原的形态学。颗粒状糖原负染的电子显微镜研究]
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6
Interpretation of electron micrographs of single and serial sections.单张切片和连续切片电子显微镜照片的解读。
J Biophys Biochem Cytol. 1955 Jul 25;1(4):301-14. doi: 10.1083/jcb.1.4.301.
7
STAINING THIN SECTIONS WITH LEAD HYDROXIDE WITHOUT CONTAMINATION BY PRECIPITATED LEAD CARBONATE.用氢氧化铅对薄片进行染色,避免被碳酸铅沉淀污染。
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Reduction of heating artifacts in thin sections examined in the electron microscope.减少在电子显微镜下检查的薄片中的加热伪像。
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FINE STRUCTURE OF THE NEUROHYPOPHYSIS OF THE OPOSSUM (DIDELPHIS VIRGINIANA).负鼠(弗吉尼亚负鼠)神经垂体的精细结构
J Cell Biol. 1964 Mar;20(3):459-72. doi: 10.1083/jcb.20.3.459.
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Light and electron microscopic observation of specific atrial granules using water-miscible resin as an embedding medium.使用水溶性树脂作为包埋介质对特定心房颗粒进行光镜和电镜观察。
Acta Med Okayama. 1988 Dec;42(6):311-6. doi: 10.18926/AMO/31003.

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本文引用的文献

1
The accumulation of glycogen in the glycogen body of the nerve cord of the developing chick.糖原在发育中雏鸡神经索糖原体内的积累。
J Morphol. 1949 Sep;85(2):391-403. doi: 10.1002/jmor.1050850205.
2
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
3
An electron microscope study of the early effects of 3'-Me-DAB on rat liver cells.3'-甲基二乙基亚硝胺对大鼠肝细胞早期影响的电子显微镜研究。
Cancer Res. 1959 Nov;19:997-1009.
4
Permanganate fixation of plant cells.植物细胞的高锰酸盐固定
J Biophys Biochem Cytol. 1959 Dec;6(3):431-6. doi: 10.1083/jcb.6.3.431.
5
A small particulate component of the cytoplasm.细胞质的一种小颗粒成分。
J Biophys Biochem Cytol. 1955 Jan;1(1):59-68. doi: 10.1083/jcb.1.1.59.
6
A device for staining tissue sections for electron microscopy.一种用于电子显微镜检查的组织切片染色装置。
J Biophys Biochem Cytol. 1959 May 25;5(3):511-3. doi: 10.1083/jcb.5.3.511.
7
The development of the cnidoblasts of Hydra; an electron microscope study of cell differentiation.水螅刺细胞的发育;细胞分化的电子显微镜研究
J Biophys Biochem Cytol. 1959 May 25;5(3):441-52. doi: 10.1083/jcb.5.3.441.
8
Intracellular impulse conduction in muscle cells.肌肉细胞内的冲动传导。
Science. 1959 Mar 13;129(3350):721-2. doi: 10.1126/science.129.3350.721.
9
Staining of tissue sections for electron microscopy with heavy metals. II. Application of solutions containing lead and barium.用于电子显微镜检查的重金属组织切片染色。II. 含铅和钡溶液的应用。
J Biophys Biochem Cytol. 1958 Nov 25;4(6):727-30. doi: 10.1083/jcb.4.6.727.
10
Araldite as an embedding medium for electron microscopy.用于电子显微镜的环氧树脂包埋介质。
J Biophys Biochem Cytol. 1958 Mar 25;4(2):191-4. doi: 10.1083/jcb.4.2.191.

在薄组织切片的电子显微照片中鉴定糖原。

Identification of glycogen in electron micrographs of thin tissue sections.

作者信息

REVEL J P, NAPOLITANO L, FAWCETT D W

出版信息

J Biophys Biochem Cytol. 1960 Dec;8(3):575-89. doi: 10.1083/jcb.8.3.575.

DOI:10.1083/jcb.8.3.575
PMID:13741016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2224957/
Abstract

The electron microscopic appearance of glycogen has been studied in the organs of several animal species. Glycogen almost always appears as roughly circular granules from 150 to 400 A in diameter. The intrinsic electron density of glycogen varies from tissue to tissue; however, treatment with lead hydroxide as described by Watson deeply stains the granules. Glycogen pellets were isolated from some of the tissues studied by centrifugation. Such pellets were shown to be glycogen by chemical and histochemical criteria. When thin sections of the pellet are examined under the electron microscope they can be seen to consist of densely packed granules similar to those found in the intact tissues. Such pellets are also stained for electron microscopy by short exposure to lead hydroxide.

摘要

已对几种动物物种器官中糖原的电子显微镜外观进行了研究。糖原几乎总是呈现为直径150至400埃的大致圆形颗粒。糖原的固有电子密度因组织而异;然而,按照沃森所述用氢氧化铅处理会使颗粒深度染色。通过离心从一些研究的组织中分离出糖原沉淀。通过化学和组织化学标准证明这些沉淀是糖原。当在电子显微镜下检查沉淀的薄片时,可以看到它们由紧密堆积的颗粒组成,类似于在完整组织中发现的颗粒。通过短时间暴露于氢氧化铅,这些沉淀也可用于电子显微镜染色。