Manual of Methods for General Bacteriology |
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Page 144
... to dissolve the agar completely . If heated over a flame or on a hot plate , stir
the medium constantly during heating to prevent the agar from settling to the
bottom of the pan where it can caramelize and char ; then bring the medium to a ...
... to dissolve the agar completely . If heated over a flame or on a hot plate , stir
the medium constantly during heating to prevent the agar from settling to the
bottom of the pan where it can caramelize and char ; then bring the medium to a ...
Page 153
In fresh medium , the length of the lag phase depends upon the size of the
inoculum , the age ... A small inoculum volume transferred to a large volume of
fresh medium may result in outward diffusion of vitamins , cofactors , and ions
which are ...
In fresh medium , the length of the lag phase depends upon the size of the
inoculum , the age ... A small inoculum volume transferred to a large volume of
fresh medium may result in outward diffusion of vitamins , cofactors , and ions
which are ...
Page 163
CHEMOSTAT 163 Medium flow pipette . Open pinch clamp C and close pinch
clamp A to resume normal operation . The dilution rate ( or specific growth rate for
single culture vessels without recycle ) is then calculated by dividing the flow rate
...
CHEMOSTAT 163 Medium flow pipette . Open pinch clamp C and close pinch
clamp A to resume normal operation . The dilution rate ( or specific growth rate for
single culture vessels without recycle ) is then calculated by dividing the flow rate
...
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Contents
55 | 32 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
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Common terms and phrases
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 enrichment 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 mg/liter microscopy mixture mutants 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