Manual of Methods for General Bacteriology |
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Page 368
Most of the other techniques have ally hydrolases such as alkaline phosphatase ,
specialized uses or are effective only with orgaribonuclease I , and cyclic
phosphodiesterase . nisms ( such as protozoans or animal tissues ) The method
...
Most of the other techniques have ally hydrolases such as alkaline phosphatase ,
specialized uses or are effective only with orgaribonuclease I , and cyclic
phosphodiesterase . nisms ( such as protozoans or animal tissues ) The method
...
Page 369
This , comNossal ( McDonald Engineering Co. , Bay Village , bined with its
effectiveness in breaking a wide Ohio ) instruments ... A much more effective
techsound is caused by cavitational forces producing nique for solid shear
disruption of ...
This , comNossal ( McDonald Engineering Co. , Bay Village , bined with its
effectiveness in breaking a wide Ohio ) instruments ... A much more effective
techsound is caused by cavitational forces producing nique for solid shear
disruption of ...
Page 501
organisms , and can effective duration of contact be maintained ? What
restrictions apply with respect to compatibility of materials ? What is the stability of
the disinfectant in use concentrations , and does the anticipated use situation
require ...
organisms , and can effective duration of contact be maintained ? What
restrictions apply with respect to compatibility of materials ? What is the stability of
the disinfectant in use concentrations , and does the anticipated use situation
require ...
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Contents
MORPHOLOGY | 5 |
Specimen Preparation for Light Microscopy R G E MURRAY AND C F ROBI | 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