Physical Principles and Techniques of Protein ChemistryPhysical Principles and Techniques of Protein Chemistry Part C ... |
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Page 7
Comparison of Mechanisms Which Effect Contrast in the Light and Electron
Microscopes The origin of observed contrast must be considered in interpretating
a microscope image . In the ordinary light microscope , contrast is achieved ...
Comparison of Mechanisms Which Effect Contrast in the Light and Electron
Microscopes The origin of observed contrast must be considered in interpretating
a microscope image . In the ordinary light microscope , contrast is achieved ...
Page 9
The scattering contrast of specimens of low average atomic number can be
enhanced instrumentally by the use of a limiting objective aperture . The aperture
of the objective lenses of electron microscopes is somewhat larger in practice
than ...
The scattering contrast of specimens of low average atomic number can be
enhanced instrumentally by the use of a limiting objective aperture . The aperture
of the objective lenses of electron microscopes is somewhat larger in practice
than ...
Page 31
contrast ( Levin , 1963a ) whereas the larger but more penetrable serum albumin
molecule ( M . W . 66 , 000 ) tends to remain invisible in similar preparations . An
interesting example of the uncertainties of interpreting negativecontrast images ...
contrast ( Levin , 1963a ) whereas the larger but more penetrable serum albumin
molecule ( M . W . 66 , 000 ) tends to remain invisible in similar preparations . An
interesting example of the uncertainties of interpreting negativecontrast images ...
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Contents
The Enhancement of Contrast | 21 |
The Preservation of Specimens | 35 |
Examples of the Application of Electron Microscopy to the Study | 48 |
Copyright | |
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absorbance absorption acid appears applied atoms axis binding birefringence boundary buffer calculated cell charge Chem chromophores complex concentration constant containing contrast corrected corresponding curve decrease dependence determined dielectric difference diffusion dipole direction discussed distribution effect electric electric field electron electrophoresis emission energy equation equilibrium example excitation experimental experiments factor fluorescence fraction frequency function given groups Herskovits important increase indicates intensity interactions ionic ions length light limited macromolecules measured method mobility molecular molecules observed obtained occurs optical orientation particles patterns peaks perturbation phase phenolic polarization position possible preparation present produced protein quantum range ratio reaction reference relative relaxation respectively rotation sample separation serum albumin shift shown single solution solvent specimen spectra spectrum strength structure studies technique temperature theory tion transfer transition tryptophan unit usually volume wavelength yield zone