Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 33
Page 250
These latter two methods generally prevent infection of potential transductants by
phage released from recipient cells that were productively infected .
Transductants are recovered and enumerated by plating on appropriate selective
media .
These latter two methods generally prevent infection of potential transductants by
phage released from recipient cells that were productively infected .
Transductants are recovered and enumerated by plating on appropriate selective
media .
Page 255
When using the lysogenic recipient , double infections will not decrease the
recovery of transductants since the lysogenic cells are ... 2 M sodium citrate to
each phage - bacteria mixture to chelate the Ca2 + and stop further infection of
P1 . 6 .
When using the lysogenic recipient , double infections will not decrease the
recovery of transductants since the lysogenic cells are ... 2 M sodium citrate to
each phage - bacteria mixture to chelate the Ca2 + and stop further infection of
P1 . 6 .
Page 487
GENERAL LABORATORY PRACTICES A summary and analysis of 3 , 921 cases
of laboratory - associated infections were reported by Pike ( 11 ) , and the cases
... Such accounts indi - cate that individuals working with bacteria risk infection ...
GENERAL LABORATORY PRACTICES A summary and analysis of 3 , 921 cases
of laboratory - associated infections were reported by Pike ( 11 ) , and the cases
... Such accounts indi - cate that individuals working with bacteria risk infection ...
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