Manual of Methods for General Bacteriology |
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Page 295
is necessary , the measurements needed being Assembly of electrode
membrane . differences between experimental samples . For The demanding
aspect of the Clark electrode example , if Ringer's solution contains 5 ul of Oz / is
attaching ...
is necessary , the measurements needed being Assembly of electrode
membrane . differences between experimental samples . For The demanding
aspect of the Clark electrode example , if Ringer's solution contains 5 ul of Oz / is
attaching ...
Page 308
This can be prevented sample size also dictates initial bandwidth , by making a
loop in the outlet tube which is length and diameter become functions of the
higher than the gel surface . degree of separation needed for a given sample
volume ...
This can be prevented sample size also dictates initial bandwidth , by making a
loop in the outlet tube which is length and diameter become functions of the
higher than the gel surface . degree of separation needed for a given sample
volume ...
Page 317
In addition , inhomogeneity of solutions or counting of paper strips produces
errors . Long counts are not needed at low radioactivity levels as for the channel
ratio method . It is possible to improve the external standard method described
above ...
In addition , inhomogeneity of solutions or counting of paper strips produces
errors . Long counts are not needed at low radioactivity levels as for the channel
ratio method . It is possible to improve the external standard method described
above ...
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Contents
MORPHOLOGY | 5 |
Specimen Preparation for Light Microscopy R G E MURRAY AND C F ROBI | 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