Manual of Methods for General Bacteriology |
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Page 310
... and licensing and periodic inspec- labeling is of very high specific activity ; these tion are usually required for the parent institurequire special precautions . ' * C , although a weak tion under which the research is conducted .
... and licensing and periodic inspec- labeling is of very high specific activity ; these tion are usually required for the parent institurequire special precautions . ' * C , although a weak tion under which the research is conducted .
Page 377
In addirelating absorbancy at 540 nm to concentration tion , the assay can be conducted using whole of L - ribulose under these conditions . cells made permeable to the reactants by treatment with hexadecyltrimethylammonium bro18.2.11 .
In addirelating absorbancy at 540 nm to concentration tion , the assay can be conducted using whole of L - ribulose under these conditions . cells made permeable to the reactants by treatment with hexadecyltrimethylammonium bro18.2.11 .
Page 481
The time required for sterilization is apColorless gas at ambient temperature proximately halved by doubling the concentraBoiling point , 10.8 ° C tion of Eto , and the temperature coefficient of Very reactive alkylating agent the ...
The time required for sterilization is apColorless gas at ambient temperature proximately halved by doubling the concentraBoiling point , 10.8 ° C tion of Eto , and the temperature coefficient of Very reactive alkylating agent 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