Manual of Methods for General Bacteriology |
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Page 54
Neither of these devices had any provision The major disadvantage is that
breakage is for cooling the sample during shaking , and it was not instantaneous
, and a cell suspension must be necessary to interrupt the shaking frequently to ...
Neither of these devices had any provision The major disadvantage is that
breakage is for cooling the sample during shaking , and it was not instantaneous
, and a cell suspension must be necessary to interrupt the shaking frequently to ...
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 356
Since mation ; then slowly pour in the Cd - Cu filings the analysis is for total NO2 ,
part of the sample and let them ... Sampling . Procedure . Add 2 ml of
concentrated NH CI Samples should be treated as described above reagent to
100 ml of ...
Since mation ; then slowly pour in the Cd - Cu filings the analysis is for total NO2 ,
part of the sample and let them ... Sampling . Procedure . Add 2 ml of
concentrated NH CI Samples should be treated as described above reagent to
100 ml of ...
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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