Physical Principles and Techniques of Protein ChemistryPhysical Principles and Techniques of Protein Chemistry Part C ... |
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Page 73
The electron density p ( xyz ) at a point in the unit cell with fractional coordinates
X , y , z may be calculated by summing the triple series p ( xyz ) = F ( hkl ) exp ( -
21i ( hx + ky + lz ) ] ( 6 ) - k = - 1 =where V is the volume of the unit cell and F ( hkl
) ...
The electron density p ( xyz ) at a point in the unit cell with fractional coordinates
X , y , z may be calculated by summing the triple series p ( xyz ) = F ( hkl ) exp ( -
21i ( hx + ky + lz ) ] ( 6 ) - k = - 1 =where V is the volume of the unit cell and F ( hkl
) ...
Page 118
The optical density is proportional to concentration , c , of absorber ( Beer ' s law )
and path length , 1 , of absorber ( Lambert ' s law ) : D = ecl . The proportionality
constant e is called the molar absorption coefficient when the absorber ...
The optical density is proportional to concentration , c , of absorber ( Beer ' s law )
and path length , 1 , of absorber ( Lambert ' s law ) : D = ecl . The proportionality
constant e is called the molar absorption coefficient when the absorber ...
Page 191
When 5 % light absorption occurs , the optical density is given by OD = log 100 /
95 = 0 . 022 . Under these conditions the optical density per centimeter path
length of solution , measured in a 1 x 1 cm fluorescence cell , is 0 . 022 / 0 . 5 = 0 .
When 5 % light absorption occurs , the optical density is given by OD = log 100 /
95 = 0 . 022 . Under these conditions the optical density per centimeter path
length of solution , measured in a 1 x 1 cm fluorescence cell , is 0 . 022 / 0 . 5 = 0 .
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Contents
The Enhancement of Contrast | 21 |
The Preservation of Specimens | 35 |
Examples of the Application of Electron Microscopy to the Study | 48 |
Copyright | |
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absorbance absorption acid appears applied atoms axis binding birefringence boundary buffer calculated cell charge Chem chromophores complex concentration constant containing contrast corrected corresponding curve decrease dependence determined dielectric difference diffusion dipole direction discussed distribution effect electric electric field electron electrophoresis emission energy equation equilibrium example excitation experimental experiments factor fluorescence fraction frequency function given groups Herskovits important increase indicates intensity interactions ionic ions length light limited macromolecules measured method mobility molecular molecules observed obtained occurs optical orientation particles patterns peaks perturbation phase phenolic polarization position possible preparation present produced protein quantum range ratio reaction reference relative relaxation respectively rotation sample separation serum albumin shift shown single solution solvent specimen spectra spectrum strength structure studies technique temperature theory tion transfer transition tryptophan unit usually volume wavelength yield zone