Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 79
Page 58
Ionic detergents bind lem by labeling cultures with a small amount of strongly to proteins , and in the case of SDS this [ H ] ... per milligram of protein is constant practical because of extensive protein binding . throughout growth .
Ionic detergents bind lem by labeling cultures with a small amount of strongly to proteins , and in the case of SDS this [ H ] ... per milligram of protein is constant practical because of extensive protein binding . throughout growth .
Page 323
for each protein and standard run at several gel concentrations , i.e. , at different degrees of crosslinking ( Fig . 12A ) . These plots are linear , and plots of their slopes versus molecular weight are also linear .
for each protein and standard run at several gel concentrations , i.e. , at different degrees of crosslinking ( Fig . 12A ) . These plots are linear , and plots of their slopes versus molecular weight are also linear .
Page 358
The reactivity 500 nm for those with high NH « * ( 250 to 500 ug / of this reagent to freshly added protein lasts 50 ml ) . This reaction can be used with propor- only seconds after dilution . After 30 min or tionally smaller volumes of ...
The reactivity 500 nm for those with high NH « * ( 250 to 500 ug / of this reagent to freshly added protein lasts 50 ml ) . This reaction can be used with propor- only seconds after dilution . After 30 min or tionally smaller volumes of ...
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
Bibliographic information
| Title | Manual of Methods for General Bacteriology |
| Authors | Philipp Gerhardt, American Society for Microbiology |
| Editor | Philipp Gerhardt |
| Edition | illustrated |
| Publisher | American Society for Microbiology, 1981 |
| Original from | the University of Michigan |
| Digitized | 17 Jul 2008 |
| ISBN | 0914826301, 9780914826309 |
| Length | 524 pages |
| Subjects | › Science / General |
| Export Citation | BiBTeX EndNote RefMan |