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- W3036765233 abstract "When tissue is prepared for thin section, high resolution electron microscopy with the specific goal of minimally denaturing membrane protein and with the least lipid solubilization possible, the method of choice is cross-linking membrane protein with a short exposure to 1% glutaraldehyde, brief dehydration in O°C ethylene glycol, and Vestopal infiltration. After such a procedure, the resultant contrast, even after uranyl acetate section staining, is extremely low. This low contrast is due to the few charged groups on native proteins available for interaction with the stain and the protein's compact structure which prohibits stain ions from penetrating into the nonpolar interior. To optimally increase the resultant low contrast in an effort to study the complex, three dimensional, condensed state of heterogeneous membrane proteins (10-100A) in the 300A-thick mitochondrial inner membranes (Figures 1-2) and the 270A-thick chloroplast partition membranes, sections were mounted over Triafol nets (Figure 3) spanning one hole slot grids." @default.
- W3036765233 created "2020-06-25" @default.
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- W3036765233 date "1973-08-01" @default.
- W3036765233 modified "2023-10-14" @default.
- W3036765233 title "Contrast Enhancement of Glutaraldehyde Cross-Linked, Ethylene Glycol Dehydrated Tissue With Triafol Nets" @default.
- W3036765233 doi "https://doi.org/10.1017/s0424820100072058" @default.
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