Manual of Methods for General Bacteriology |
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Page 167
Step or pulse changes in the uisites are met , establish batch cultivation conculture environment can trigger spore germina- ditions so that two to five cell mass doublings tion and may actually closely model natural during logarithmic ...
Step or pulse changes in the uisites are met , establish batch cultivation conculture environment can trigger spore germina- ditions so that two to five cell mass doublings tion and may actually closely model natural during logarithmic ...
Page 367
ically appropriate environment containing chlor- not gain entry through the cell wall - membrane amphenicol ( ca. ... Solvent ( toluene or benzene ) In other cases , it is imperative that the cells treatment has been successfully used ...
ically appropriate environment containing chlor- not gain entry through the cell wall - membrane amphenicol ( ca. ... Solvent ( toluene or benzene ) In other cases , it is imperative that the cells treatment has been successfully used ...
Page 506
Volume The volume of a mass of wet cells ( or the average size of a single cell ) is best obtained by the procedure described in 19.1 . 300 25.2.5 . Wet and Dry Densities Water content ( % dry weight ) a The density ( essentially the ...
Volume The volume of a mass of wet cells ( or the average size of a single cell ) is best obtained by the procedure described in 19.1 . 300 25.2.5 . Wet and Dry Densities Water content ( % dry weight ) a The density ( essentially the ...
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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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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