Manual of Methods for General Bacteriology |
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Page 161
Comparison of chemostat and turbidostat Operating parameter Chemostat Turbidostat Operation at or near maximum Unstable Stable , very nearly steady state specific growth rate Operation at low specific growth Stable steady states ...
Comparison of chemostat and turbidostat Operating parameter Chemostat Turbidostat Operation at or near maximum Unstable Stable , very nearly steady state specific growth rate Operation at low specific growth Stable steady states ...
Page 310
H as strictly regulated by the Nuclear Regulatory in ' H2O is volatile , and ' H2 gas used in compound Commission , and licensing and periodic inspec- labeling is of very high specific activity ; these tion are usually required for the ...
H as strictly regulated by the Nuclear Regulatory in ' H2O is volatile , and ' H2 gas used in compound Commission , and licensing and periodic inspec- labeling is of very high specific activity ; these tion are usually required for the ...
Page 311
Determination of total ' ' C radioactiv . from high specific activities . This process can be ity of the pure isolated compound measures the minimized by adherence to the specific condi- recovery of the sterol in the procedure .
Determination of total ' ' C radioactiv . from high specific activities . This process can be ity of the pure isolated compound measures the minimized by adherence to the specific condi- recovery of the sterol in the procedure .
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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