Manual of Methods for General Bacteriology |
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Page 355
Neutralization of all have been commonly used for the reduction of samples to pH
7.0 is suggested before analysis . NO3- to NO2 , reduction by zinc ( 81 , 92 ) and
reduction by cadmium ( 68 , 86 ) ; both are deReagents . scribed here .
Neutralization of all have been commonly used for the reduction of samples to pH
7.0 is suggested before analysis . NO3- to NO2 , reduction by zinc ( 81 , 92 ) and
reduction by cadmium ( 68 , 86 ) ; both are deReagents . scribed here .
Page 356
After either of the reduction procedures de column with dilute NHCl solution or
with the scribed here , the analysis for NO2 ... and let them settle until a column
height of must be analyzed for NO2 before reduction , and about 30 cm is
achieved .
After either of the reduction procedures de column with dilute NHCl solution or
with the scribed here , the analysis for NO2 ... and let them settle until a column
height of must be analyzed for NO2 before reduction , and about 30 cm is
achieved .
Page 360
AcetWhen preservation of a protein sample is im- ylene reduction is usually
tested in systems that portant because of its limited availability , this have
sufficient nitrogenase activity to allow a nondestructive assay procedure is the
method of ...
AcetWhen preservation of a protein sample is im- ylene reduction is usually
tested in systems that portant because of its limited availability , this have
sufficient nitrogenase activity to allow a nondestructive assay procedure is the
method of ...
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Contents
MORPHOLOGY | 5 |
NOW | 17 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
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 examine example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plate positive prepared present Press procedure protein reaction reagent references remove 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