Manual of Methods for General Bacteriology |
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Page 366
mation , and regulation of bacterial enzyme sys- mation as possible concerning the various reactems . tions that occur and to understand how they are The various types of cell preparation that are interwoven into the fabric of the life ...
mation , and regulation of bacterial enzyme sys- mation as possible concerning the various reactems . tions that occur and to understand how they are The various types of cell preparation that are interwoven into the fabric of the life ...
Page 370
This need to consider the effect of The choice of a cell disruption technique is protein concentration on enzyme activity ... the volume regulatory enzymes ( 28 ) . of extract required , the sensitivity of the en- If susceptibility to ...
This need to consider the effect of The choice of a cell disruption technique is protein concentration on enzyme activity ... the volume regulatory enzymes ( 28 ) . of extract required , the sensitivity of the en- If susceptibility to ...
Page 372
4 larger amounts of the auxiliary enzyme until the quite clearly the differences between enzyme linear initial velocity of the primary reaction can activity on the one hand and enzyme specific be determined accurately .
4 larger amounts of the auxiliary enzyme until the quite clearly the differences between enzyme linear initial velocity of the primary reaction can activity on the one hand and enzyme specific be determined accurately .
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Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
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Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York