Physical Principles and Techniques of Protein ChemistrySydney J. Leach Physical Principles and Techniques of Protein Chemistry Part C ... |
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Page 7
... intensity . In the electron microscope , absorption of electrons is , and in fact must be , of negligible importance , since appreciable absorption of elec- trons by the specimen would lead rapidly to its thermal destruction ...
... intensity . In the electron microscope , absorption of electrons is , and in fact must be , of negligible importance , since appreciable absorption of elec- trons by the specimen would lead rapidly to its thermal destruction ...
Page 172
... intensity of emitted radiation ( in terms of quanta emitted in unit time ) probability of spontaneous transition number of excited molecules at equilibrium " natural " lifetime of the excited state in the absence of perturbations ...
... intensity of emitted radiation ( in terms of quanta emitted in unit time ) probability of spontaneous transition number of excited molecules at equilibrium " natural " lifetime of the excited state in the absence of perturbations ...
Page 189
... Intensity While the intensity of fluorescence of a sample can be measured ex- actly , for many purposes it is sufficient merely to obtain a quantity , the " observed fluorescence intensity , " expressed in arbitrary detector units . For ...
... Intensity While the intensity of fluorescence of a sample can be measured ex- actly , for many purposes it is sufficient merely to obtain a quantity , the " observed fluorescence intensity , " expressed in arbitrary detector units . For ...
Contents
Electron Microscopy | 2 |
Ultraviolet Absorption | 3 |
Dielectric Properties of Proteins | 7 |
Copyright | |
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absorption absorption spectrum amino acids applied atoms axis Biochem Biol Biophys birefringence boundary bovine serum albumin buffer calculated Cann cell Chem chromophores coefficient components concentration curve Debye denaturation density determined dielectric constant dielectric increment dielectric relaxation difference spectrum dipole moment Edelhoch effects electric birefringence electric field electron microscope electrophoresis elution volume emission enzyme equation equilibrium excitation experimental film fluorescence fraction frequency gel filtration gradient groups instrument intensity interactions ionic strength ions lens light linear macromolecules magnification measured method micrographs migration mobility molar molecular weight molecules moving-boundary observed obtained optical ovalbumin parameter particles peaks permanent dipole perturbation phase phenolic photomultiplier Phys plot polarization polymer produced protein quantum yield ratio reaction relaxation residues resolution resolving power ribonuclease scattering shadow shown in Fig solution solvent specimen spectra structure studies technique temperature theoretical theory tion tryptophan tyrosine values wavelength Weber Winzor zone