Physical Principles and Techniques of Protein ChemistrySydney J. Leach Physical Principles and Techniques of Protein Chemistry Part C ... |
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Page 83
... peaks appear close to the true positions of the lighter atoms . The peaks associated with the hydrogen atoms are very weak and are lost in the spurious background . The accuracy of the map can be improved by Fourier refinement . In ...
... peaks appear close to the true positions of the lighter atoms . The peaks associated with the hydrogen atoms are very weak and are lost in the spurious background . The accuracy of the map can be improved by Fourier refinement . In ...
Page 405
... peaks even for very rapid reequili- bration . The implications for conventional electrophoretic analysis have already been touched upon and will be developed more fully below . Finally , the new understanding provided by these ...
... peaks even for very rapid reequili- bration . The implications for conventional electrophoretic analysis have already been touched upon and will be developed more fully below . Finally , the new understanding provided by these ...
Page 408
... peaks but only a single broad descending one ) is shown typically by a variety of proteins in media containing 0.01 M sodium acetate buffer . In addition , the theory accounts for ( 1 ) the progressive changes induced in the patterns by ...
... peaks but only a single broad descending one ) is shown typically by a variety of proteins in media containing 0.01 M sodium acetate buffer . In addition , the theory accounts for ( 1 ) the progressive changes induced in the patterns by ...
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