Manual of Methods for General Bacteriology |
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Page 252
They can be purified on MA + Gal , EMB + Gal , or MacConkey + Gal plates which
should of course , be incubated at ... to grow at 37 or 42°C . This can be tested by
spotting loopfuls of each culture on an EMB + Gal plate and incubating at 37 or ...
They can be purified on MA + Gal , EMB + Gal , or MacConkey + Gal plates which
should of course , be incubated at ... to grow at 37 or 42°C . This can be tested by
spotting loopfuls of each culture on an EMB + Gal plate and incubating at 37 or ...
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 . Free - Solution Method action vials for 1 to 2 h ,
treat 25 ul of the sample Free - solution reassociation of denatured DNA with 5 to
10 % trichloroacetic acid , collect the fragments can be measured optically by ...
After incubating the re 22 . 6 . 4 . Free - Solution Method action vials for 1 to 2 h ,
treat 25 ul of the sample Free - solution reassociation of denatured DNA with 5 to
10 % trichloroacetic acid , collect the fragments can be measured optically by ...
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Contents
55 | 32 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
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 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