Manual of Methods for General Bacteriology |
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Page 277
Values in the column were obtained by subtracting the value in line 2 from the respective values in lines 3 , 4 , and 5 and then normalizing to the corrected value in line 3 . ༄༅ * » ན་ ds SS Fig . 5. Heteroduplexing.
Values in the column were obtained by subtracting the value in line 2 from the respective values in lines 3 , 4 , and 5 and then normalizing to the corrected value in line 3 . ༄༅ * » ན་ ds SS Fig . 5. Heteroduplexing.
Page 450
A DNA homology values are average measurecrude comparison can be made with respect to ments of similarity which use the entire genome the overall DNA base composition : of the total of each organism being compared .
A DNA homology values are average measurecrude comparison can be made with respect to ments of similarity which use the entire genome the overall DNA base composition : of the total of each organism being compared .
Page 466
If the logs of the x values are plotted , when y = 1/2 , log a = log 1 / X1 / 2 -log X1 / 2 . A general log Cot plot is shown in Fig . 9. There is an almost linear region on the curve that extends for about 2 logs .
If the logs of the x values are plotted , when y = 1/2 , log a = log 1 / X1 / 2 -log X1 / 2 . A general log Cot plot is shown in Fig . 9. There is an almost linear region on the curve that extends for about 2 logs .
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Contents
1 | 22 |
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 amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York