Physical Principles and Techniques of Protein ChemistrySydney J. Leach Physical Principles and Techniques of Protein Chemistry Part C ... |
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Page 50
... length of fibrinogen molecules as a function of pH seems to indicate that contraction of the molecule to a length of 230 Å is in fact possible ( H. S. Slayter and Hall , 1962 ) . Measurements from electron micrographs , of specimens ...
... length of fibrinogen molecules as a function of pH seems to indicate that contraction of the molecule to a length of 230 Å is in fact possible ( H. S. Slayter and Hall , 1962 ) . Measurements from electron micrographs , of specimens ...
Page 163
... length cell and a more concentrated solution in a short - path - length cell ( Section VI , G ) , or merely to use short - path - length cells because other experimental condi- tions ( e.g. , high concentration ) require the use of ...
... length cell and a more concentrated solution in a short - path - length cell ( Section VI , G ) , or merely to use short - path - length cells because other experimental condi- tions ( e.g. , high concentration ) require the use of ...
Page 191
... length of solution , measured in a 1 X 1 cm fluorescence cell , is 0.022 / 0.5 = 0.044 . However , if an 0.29 × 0.29 cm microcell is used , a much more concen- trated solution can be used whose optical density per centimeter path length ...
... length of solution , measured in a 1 X 1 cm fluorescence cell , is 0.022 / 0.5 = 0.044 . However , if an 0.29 × 0.29 cm microcell is used , a much more concen- trated solution can be used whose optical density per centimeter path length ...
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