Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 79
Page 159
Absolute exclusion of oxygen from acid , base , or other solutions to be added to the fermentor in small quantities is not necessary since the reducing characteristics of an active anaerobic culture will adequately cope with very slight ...
Absolute exclusion of oxygen from acid , base , or other solutions to be added to the fermentor in small quantities is not necessary since the reducing characteristics of an active anaerobic culture will adequately cope with very slight ...
Page 311
cpm added = a chemical purities of a compound may occur dur- instance , ' C - sterol of known total activity can ing storage , due primarily to radiation damage be added . Determination of total ' ' C radioactiv . from high specific ...
cpm added = a chemical purities of a compound may occur dur- instance , ' C - sterol of known total activity can ing storage , due primarily to radiation damage be added . Determination of total ' ' C radioactiv . from high specific ...
Page 425
Make up the volume in each tube to 0.10 of 20 microtubes containing various dehydrated ml by adding 0.08 , 0.06 , 0.04 ... Evaluations of reliability may be found in NAD was added to the first tube . references 16 , 31 , 40 , 68-70 ...
Make up the volume in each tube to 0.10 of 20 microtubes containing various dehydrated ml by adding 0.08 , 0.06 , 0.04 ... Evaluations of reliability may be found in NAD was added to the first tube . references 16 , 31 , 40 , 68-70 ...
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