Physical Principles and Techniques of Protein Chemistry, Part 1 |
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Page 24
In fact , when an appropriate procedure is once ed out for use with a particular
vacuum evaporator , the method is not only extremely simple , but also
remarkably reliable in routine use . Important considerations in establishing a
standard ...
In fact , when an appropriate procedure is once ed out for use with a particular
vacuum evaporator , the method is not only extremely simple , but also
remarkably reliable in routine use . Important considerations in establishing a
standard ...
Page 458
procedure , the essential features of which may be summarized as follows . A
weighed amount of gel is allowed to swell in the appropriate buffer , after which a
known amount ( Qt ) of protein is added . Ky is then calculated from Eq . ( 6 ) K ...
procedure , the essential features of which may be summarized as follows . A
weighed amount of gel is allowed to swell in the appropriate buffer , after which a
known amount ( Qt ) of protein is added . Ky is then calculated from Eq . ( 6 ) K ...
Page 471
The superiority of this procedure over method A is demonstrated by the
redundancy of the distinction between glycoproteins and carbohydrate - free
globular proteins when elution volume is plotted against the reciprocal of the
diffusion ...
The superiority of this procedure over method A is demonstrated by the
redundancy of the distinction between glycoproteins and carbohydrate - free
globular proteins when elution volume is plotted against the reciprocal of the
diffusion ...
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Contents
LIST OF CONTRIBUTORS | 2 |
The Enhancement of Contrast | 21 |
The Preservation of Specimens | 35 |
Copyright | |
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Common terms and phrases
absorbance absorption acid appears applied atoms axis birefringence boundary buffer calculated cell charge Chem chromophores complex concentration constant containing contrast corrected corresponding curve dependence determined dielectric difference diffusion dipole direction distribution effects electric electric field electron electrophoresis elution emission energy equation equilibrium example excitation experimental experiments factor flow fluorescence fraction frequency function gel filtration given groups important increase indicates intensity interactions ionic ions length light limited macromolecules measured method microscope migration mobility molecular molecules myosin observed obtained occurs optical particles patterns peaks perturbation phase plot polarization position possible preparation present produced protein range ratio reaction reference relative relaxation respectively rotation scattering separation serum albumin shift shown single solution solvent specimen spectra spectrum strength structure studies technique theoretical theory tion unit usually values volume wavelength weight yield zone