Manual of Methods for General Bacteriology |
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Page 252
1 gal transducing phage genome , and some of these can be analyzed by
incubating cultures at Characterization of ... or MacConkey + Gal plates which
should , test tubes , ( ii ) incubating these subcultures at of course , be incubated
at 30 ° C ...
1 gal transducing phage genome , and some of these can be analyzed by
incubating cultures at Characterization of ... or MacConkey + Gal plates which
should , test tubes , ( ii ) incubating these subcultures at of course , be incubated
at 30 ° C ...
Page 396
After mixing of pellet and solution , the dextran preparation are sufficiently large
to be suspension should be incubated for a ... terium , it is necessary to determine
the dextran has in fact been reached during the incubation exclusion threshold .
After mixing of pellet and solution , the dextran preparation are sufficiently large
to be suspension should be incubated for a ... terium , it is necessary to determine
the dextran has in fact been reached during the incubation exclusion threshold .
Page 462
After incubating the re 22.6.4 . ... and measure the radioactivity in a scintillation
counter using an appropriate cockDNA ( a very small amount ) to be incubated
with a large excess of unlabeled DNA fragments . tail for aqueous samples .
After incubating the re 22.6.4 . ... and measure the radioactivity in a scintillation
counter using an appropriate cockDNA ( a very small amount ) to be incubated
with a large excess of unlabeled DNA fragments . tail for aqueous samples .
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Contents
MORPHOLOGY | 5 |
NOW | 17 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Copyright | |
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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