Manual of Methods for General Bacteriology |
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Page 270
... i.e. , the larger the molecular to obtain the small amount of fluid remaining in
weight , the slower the rate of migration . ... 2.5 Plasmid DNA obtained by this
method should mM disodium EDTA , and 8.9 mm boric acid ) . be further purified
for ...
... i.e. , the larger the molecular to obtain the small amount of fluid remaining in
weight , the slower the rate of migration . ... 2.5 Plasmid DNA obtained by this
method should mM disodium EDTA , and 8.9 mm boric acid ) . be further purified
for ...
Page 395
At 25 ° C , this weight of water would occupy a volume of 47.249 ml , based on
the water density at that temperature obtained from tables in a standard chemical
handbook . Therefore , the pellet volume must be 50.000 – 47.249 , or 2.752 ml .
At 25 ° C , this weight of water would occupy a volume of 47.249 ml , based on
the water density at that temperature obtained from tables in a standard chemical
handbook . Therefore , the pellet volume must be 50.000 – 47.249 , or 2.752 ml .
Page 506
Volume The volume of a mass of wet cells ( or the average size of a single cell )
is best obtained by the procedure described in 19.1 . 300 25.2.5 . Wet and Dry
Densities Water content ( % dry weight ) The density ( essentially the specific ...
Volume The volume of a mass of wet cells ( or the average size of a single cell )
is best obtained by the procedure described in 19.1 . 300 25.2.5 . Wet and Dry
Densities Water content ( % dry weight ) The density ( essentially the specific ...
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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