Manual of Methods for General Bacteriology |
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Page 81
Free pantothenic acid and many of its salts are very hygroscopic ; it is marketed
as the only slightly hygroscopic calcium salt which is freely soluble in water and
is stable to autoclaving . Like its more complex derivatives , pantothenic acid is ...
Free pantothenic acid and many of its salts are very hygroscopic ; it is marketed
as the only slightly hygroscopic calcium salt which is freely soluble in water and
is stable to autoclaving . Like its more complex derivatives , pantothenic acid is ...
Page 164
However , most simple media for cultivation of bacteria can be autoclaved prior to
use , but larger volumes of medium ... Take special care to ensure establishment
and maintenance of the chemically reduced state when autoclaving large ...
However , most simple media for cultivation of bacteria can be autoclaved prior to
use , but larger volumes of medium ... Take special care to ensure establishment
and maintenance of the chemically reduced state when autoclaving large ...
Page 432
1 , 000 ml field is moved into position . Note : The working dilution of the
fluorescent Combine gradients and adjust pH to 6 . 8 with antiserum should be
prepared fresh daily . The KOH . Sterilize by autoclaving . Note : Some undiluted
...
1 , 000 ml field is moved into position . Note : The working dilution of the
fluorescent Combine gradients and adjust pH to 6 . 8 with antiserum should be
prepared fresh daily . The KOH . Sterilize by autoclaving . Note : Some undiluted
...
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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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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