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Organization and Management of an Electron
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acetate acetone alcohol aldehyde alignment alkaline lead hydroxide angle aperture Araldite beam Biochem Biophys buffered capsules carbon films Chapter chromyl chloride clean condenser contamination contrast cross-linked plastics cutting speed Cytol cytomembranes damage dehydration developed difficulty diffraction dilute dissolved distilled water easily effective electron microscopy embedding emulsion Epon epoxy resins evaporated exposure final fixation floated fluid formaldehyde Formvar glass glass knives glutaraldehyde grain grids heat hole indicated instrument investigators knife edge laboratory layer material membranes methacrylate method micrographs microscope microtome minutes mixture monomer mounted negative stain objective lens operator ordinarily original osmium tetroxide Palade Parlodion particles particularly perfusion perhaps permanganate phosphotungstic acid photographic polyester polymerization Porter-Blum microtome possible prepared preserved problems produce proteins relatively removed replica resolution salt screen slide sodium sodium hydroxide solvent specimen suitable supporting film surface technique temperature thin tion tissue blocks trough ultrathin sectioning uranyl uranyl acetate Vestopal voltage