Manual of Methods for General Bacteriology |
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Page 133
HYPHOMICROBIUM MEDIUM 133 . . . . 75 ml 7 . 5 g er . . . . . . . . . . . . . . . . .
Defibrinated rabbit or sheep blood 8 . 5 . 20 . Glucose - Tryptone Agar ( 6 ) ( 20 . 3
. 7 ) . . . . . . . 25 ml Tryptone ( Difco ) or Trypticase 0 . 3 % potassium tellurite
solution ...
HYPHOMICROBIUM MEDIUM 133 . . . . 75 ml 7 . 5 g er . . . . . . . . . . . . . . . . .
Defibrinated rabbit or sheep blood 8 . 5 . 20 . Glucose - Tryptone Agar ( 6 ) ( 20 . 3
. 7 ) . . . . . . . 25 ml Tryptone ( Difco ) or Trypticase 0 . 3 % potassium tellurite
solution ...
Page 153
A small inoculum volume transferred to a large volume of fresh medium may
result in outward diffusion of vitamins , cofactors , and ions which are required for
many intracellular enzyme activities . If cells are inoculated from a rich medium to
a ...
A small inoculum volume transferred to a large volume of fresh medium may
result in outward diffusion of vitamins , cofactors , and ions which are required for
many intracellular enzyme activities . If cells are inoculated from a rich medium to
a ...
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
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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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 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