Manual of Methods for General Bacteriology |
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Page 5
And for which there is no substitute . now that the components of cells can be
resolved The light microscope is available to and to the level of macromolecules
and functional needed by all microbiologists , and because effeccomponents ,
and ...
And for which there is no substitute . now that the components of cells can be
resolved The light microscope is available to and to the level of macromolecules
and functional needed by all microbiologists , and because effeccomponents ,
and ...
Page 137
Philipp Gerhardt, American Society for Microbiology. 8 . 5 . 46 . SPHAEROTILUS
MEDIUM 137 several sterile glass beads to each bottle of me - dium . petri plate .
Allow to solidify . Use immediately or store in an anaerobic jar until needed .
Philipp Gerhardt, American Society for Microbiology. 8 . 5 . 46 . SPHAEROTILUS
MEDIUM 137 several sterile glass beads to each bottle of me - dium . petri plate .
Allow to solidify . Use immediately or store in an anaerobic jar until needed .
Page 295
295 is necessary , the measurements needed being differences between
experimental samples . For example , if Ringer ' s solution contains 5 ul of Oz / ml
when air saturated , 3 ml of solution giving an instrument response of 92 %
saturation ...
295 is necessary , the measurements needed being differences between
experimental samples . For example , if Ringer ' s solution contains 5 ul of Oz / ml
when air saturated , 3 ml of solution giving an instrument response of 92 %
saturation ...
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
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 example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method mg/liter Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts 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