Physical Principles and Techniques of Protein ChemistrySydney J. Leach Physical Principles and Techniques of Protein Chemistry Part C ... |
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Page 137
... phenolic groups into the solvent , is observed . The absorption then in- creases as more GC is added . Since all six phenolic groups are now exposed to solvent , and are consequently perturbed by the added GCI , this portion of the Ae ...
... phenolic groups into the solvent , is observed . The absorption then in- creases as more GC is added . Since all six phenolic groups are now exposed to solvent , and are consequently perturbed by the added GCI , this portion of the Ae ...
Page 144
... phenolic chromophores , some of which are known to be buried ( Herskovits and Laskowski , 1962a ) . Viscosity measurements indicate that unfolding of BSA does not begin until just over 8 molecules of DDS are bound by the protein ...
... phenolic chromophores , some of which are known to be buried ( Herskovits and Laskowski , 1962a ) . Viscosity measurements indicate that unfolding of BSA does not begin until just over 8 molecules of DDS are bound by the protein ...
Page 145
... phenolic groups is 286.0 — 0.3 = 285.7 mp , which is 0.7 mu to the red of the model compound acetyl- tyrosine ethyl ester . This may be considered the normal spectral shift resulting from covalent attachment of a phenolic group to a ...
... phenolic groups is 286.0 — 0.3 = 285.7 mp , which is 0.7 mu to the red of the model compound acetyl- tyrosine ethyl ester . This may be considered the normal spectral shift resulting from covalent attachment of a phenolic group to a ...
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