Manual of Methods for General Bacteriology |
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Page 160
Finally , the specific death rate is almost always much less than the specific
growth rate , so the death term may be ignored . Exceptions to this rule may occur
at very low growth rates , in the presence of toxic substances , or when cultivation
...
Finally , the specific death rate is almost always much less than the specific
growth rate , so the death term may be ignored . Exceptions to this rule may occur
at very low growth rates , in the presence of toxic substances , or when cultivation
...
Page 161
... very nearly steady state specific growth rate Operation at low specific growth
Stable steady states Unstable , transient with pulsatile rates response Dilution
rate equals specific Only at steady state At all times growth rate Cell
concentration at ...
... very nearly steady state specific growth rate Operation at low specific growth
Stable steady states Unstable , transient with pulsatile rates response Dilution
rate equals specific Only at steady state At all times growth rate Cell
concentration at ...
Page 311
For this , only the specific activity of the acetic anhydride is needed ; i . e . : cpm
recovered sterol recovery =cpm added amount of sterol ( umol ) umol of ' H -
compound recovery cpm of ' H / counting efficiency = S . A . of acetic anhydride (
u Ci ...
For this , only the specific activity of the acetic anhydride is needed ; i . e . : cpm
recovered sterol recovery =cpm added amount of sterol ( umol ) umol of ' H -
compound recovery cpm of ' H / counting efficiency = S . A . of acetic anhydride (
u Ci ...
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
Copyright | |
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absorbance acid activity added addition Adjust agar allow amino acids amount anaerobic applications appropriate assay autoclaving bacteria Bacteriol base broth buffer cells centrifuge colonies column components compounds concentration containing counting cover culture described determine dilution Dissolve distilled water effective electron enzyme example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method mg/liter Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts sample selection separation slide sodium solution specific staining standard sterile substrate surface suspension Table techniques temperature tion transfer tube usually values vitamin volume Wash York