Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 78
Page 277
jected to sonic treatment to obtain fragments of an approximate molecular weight of 2.5 X 10 % . ... The results are expressed as the percentage of the untreated controls normalized to the values obtained for the homologous reaction .
jected to sonic treatment to obtain fragments of an approximate molecular weight of 2.5 X 10 % . ... The results are expressed as the percentage of the untreated controls normalized to the values obtained for the homologous reaction .
Page 395
At 25 ° C , this weight of water would occupy a vol . ume 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 ...
At 25 ° C , this weight of water would occupy a vol . ume 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 ...
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 ) a The density ( essentially the ...
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 ) a The density ( essentially the ...
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
7 other sections not shown
Other editions - View all
Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York