Manual of Methods for General Bacteriology |
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Page 98
For most of these media , glucose is sterilized separately ( usually by autoclaving
) and added aseptically to a sterile solution of the other components . Other
carbohydrates , glycerol , and citric acid are utilized as well . ' Trace elements ( ug
...
For most of these media , glucose is sterilized separately ( usually by autoclaving
) and added aseptically to a sterile solution of the other components . Other
carbohydrates , glycerol , and citric acid are utilized as well . ' Trace elements ( ug
...
Page 248
Agar is added to 1.5 % for solidified media . Amino acids , purines , pyrimidines ,
and vitamins are added to optimal concentrations as appropriate ( Table 4 )
dependent upon the genotype of the recipient strain employed . Carbon sources
are ...
Agar is added to 1.5 % for solidified media . Amino acids , purines , pyrimidines ,
and vitamins are added to optimal concentrations as appropriate ( Table 4 )
dependent upon the genotype of the recipient strain employed . Carbon sources
are ...
Page 425
Make up the volume in each tube to 0.10 of 20 microtubes containing various
dehydrated ml by adding 0.08 , 0.06 ... Evaluations of reliability may be found in
NAD was added to the first tube . references 16 , 31 , 40 , 68–70 , 76 , 78 , and 81
.
Make up the volume in each tube to 0.10 of 20 microtubes containing various
dehydrated ml by adding 0.08 , 0.06 ... Evaluations of reliability may be found in
NAD was added to the first tube . references 16 , 31 , 40 , 68–70 , 76 , 78 , and 81
.
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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