Manual of Methods for General Bacteriology |
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Page 236
Incubate the plates at 30 ° C for about 18 h ml of various phage lysate dilutions (
10-5 , 10-6 , or until transductant colonies are just visible to 10-7 in L broth .
Incubate at 37 ° C for 20 min to the naked eye . allow phage adsorption . 7.
Replica ...
Incubate the plates at 30 ° C for about 18 h ml of various phage lysate dilutions (
10-5 , 10-6 , or until transductant colonies are just visible to 10-7 in L broth .
Incubate at 37 ° C for 20 min to the naked eye . allow phage adsorption . 7.
Replica ...
Page 249
Incubate the plates at 37 ° C for 1 or 2 days donor and never when the phage is
propagated as is appropriate ... On the other hand , marker and the growth rate of
the recipient with generalized transducing phages , donor gestrain . netic ...
Incubate the plates at 37 ° C for 1 or 2 days donor and never when the phage is
propagated as is appropriate ... On the other hand , marker and the growth rate of
the recipient with generalized transducing phages , donor gestrain . netic ...
Page 250
some . transducing phages can also pick up and trans for adsorption . ... Such
plasmid erally prevent infection of potential transducelements , upon introduction
into the recipient tants by phage released from recipient cells that host , become ...
some . transducing phages can also pick up and trans for adsorption . ... Such
plasmid erally prevent infection of potential transducelements , upon introduction
into the recipient tants by phage released from recipient cells that host , become ...
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Contents
MORPHOLOGY | 5 |
NOW | 17 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Copyright | |
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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 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 Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plate positive prepared present Press procedure protein reaction reagent references remove 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
Bibliographic information
| Title | Manual of Methods for General Bacteriology |
| Author | Philipp Gerhardt |
| Editor | Philipp Gerhardt |
| Contributors | R. G. E. Murray, Ralph N. Costilow, American Society for Microbiology, Willis A. Wood |
| Edition | illustrated, reprint |
| Publisher | American Society for Microbiology, 1981 |
| Original from | the University of Michigan |
| Digitized | 22 Aug 2011 |
| ISBN | 0914826298, 9780914826293 |
| Length | 524 pages |
| Export Citation | BiBTeX EndNote RefMan |