Manual of Methods for General Bacteriology |
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Page 17
LITERATURE CITED 17 18 18 18 19 19 The advent of electron microscopic
methods medium of growth , and they lie flat against the has diminished in part
the drive to gain the cover slip . Because they are usually spread from maximum
of ...
LITERATURE CITED 17 18 18 18 19 19 The advent of electron microscopic
methods medium of growth , and they lie flat against the has diminished in part
the drive to gain the cover slip . Because they are usually spread from maximum
of ...
Page 18
The the cells to the cover slip . The block may come higher concentrations are
suitable for gram - posoff by itself . Separation may be assisted by holditive
bacteria , while gram - negative bacteria may ing the cover slip down with forceps
and by ...
The the cells to the cover slip . The block may come higher concentrations are
suitable for gram - posoff by itself . Separation may be assisted by holditive
bacteria , while gram - negative bacteria may ing the cover slip down with forceps
and by ...
Page 23
When films of these colloids not run down the cover slip . The drop of sample dry ,
the similar charge on both bacterium and must be sufficiently small so that it does
not colloidal particle causes the edge of the dark contact the bottom of the well ...
When films of these colloids not run down the cover slip . The drop of sample dry ,
the similar charge on both bacterium and must be sufficiently small so that it does
not colloidal particle causes the edge of the dark contact the bottom of the well ...
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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