Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 87
Page 167
When these prerequisites are met , establish batch cultivation conditions so that
two to five cell mass doublings during ... of metabolic disturbance during
synchronization by physically selecting cells that are in similar states of the cell
growth ...
When these prerequisites are met , establish batch cultivation conditions so that
two to five cell mass doublings during ... of metabolic disturbance during
synchronization by physically selecting cells that are in similar states of the cell
growth ...
Page 367
DISINTEGRATED CELL PREPARATIONS 367 ically appropriate environment
containing chlor - not gain entry through the ... 2 ) . varying degrees of success ,
to make whole cells more permeable and thereby prepare them for Starved
resting ...
DISINTEGRATED CELL PREPARATIONS 367 ically appropriate environment
containing chlor - not gain entry through the ... 2 ) . varying degrees of success ,
to make whole cells more permeable and thereby prepare them for Starved
resting ...
Page 397
A zero value for R indicates that the cells used , there are generally no problems
due to are impermeable to the solute . Values from zero excessive leaching of
physiologically important to one indicate various degrees of penetration solutes ...
A zero value for R indicates that the cells used , there are generally no problems
due to are impermeable to the solute . Values from zero excessive leaching of
physiologically important to one indicate various degrees of penetration solutes ...
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
55 | 32 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
4 other sections not shown
Other editions - View all
Common terms and phrases
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 enrichment 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 mg/liter microscopy mixture mutants obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts 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