Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 75
Page 277
The results are expressed as the percentage of the untreated controls normalized to the values obtained for the homologous reaction . Si endonuclease reaction . Si endonuclease of very good activity can be purchased commercially ( Sigma ...
The results are expressed as the percentage of the untreated controls normalized to the values obtained for the homologous reaction . Si endonuclease reaction . Si endonuclease of very good activity can be purchased commercially ( Sigma ...
Page 328
Total Carbohydrates by Anthrone Reaction 333 .2 . Total Carbohydrates by Phenol Reaction 333 .3 . D - Glucose 334 .4 . Galactose 334 .5 . Glycogen 334 .6 . Hexosamines in Purified Peptidoglycans 335 .7 . Hexosamines in Complex Solutions ...
Total Carbohydrates by Anthrone Reaction 333 .2 . Total Carbohydrates by Phenol Reaction 333 .3 . D - Glucose 334 .4 . Galactose 334 .5 . Glycogen 334 .6 . Hexosamines in Purified Peptidoglycans 335 .7 . Hexosamines in Complex Solutions ...
Page 465
Hypothetical examples of the calculations of percent DNA homology values in the free - solution method by the hydroxylapatite ( HA ) and by the Si nuclease procedures HA procedure : Reaction vial cpm not adNet ' ; ade Adsorbed Honology ...
Hypothetical examples of the calculations of percent DNA homology values in the free - solution method by the hydroxylapatite ( HA ) and by the Si nuclease procedures HA procedure : Reaction vial cpm not adNet ' ; ade Adsorbed Honology ...
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