Manual of Methods for General Bacteriology |
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Page 5
But all levels of Uses of the light microscope to get structural microscopy play a
part in the study of bacteria information and to identify a bacterium are deand of
cell - free components , in nature as in scribed in Chapters 2 and 3 , respectively .
But all levels of Uses of the light microscope to get structural microscopy play a
part in the study of bacteria information and to identify a bacterium are deand of
cell - free components , in nature as in scribed in Chapters 2 and 3 , respectively .
Page 318
... background and 1 , 140 min for sample plus background ; for 10 % SE , 8 min
and 11 min are required , respectively . where R , and R , are the total rates and
the background rate , respectively , and t , and to are the times for R , and Ro . 16
.
... background and 1 , 140 min for sample plus background ; for 10 % SE , 8 min
and 11 min are required , respectively . where R , and R , are the total rates and
the background rate , respectively , and t , and to are the times for R , and Ro . 16
.
Page 383
Components involved in transcription of the lac operon include : the Z , Y , and A
genes containing the code for B - galactosidase , B - galactoside permease , and
B - galactoside transacetylase , respectively ; the regulatory gene ( i ) that codes ...
Components involved in transcription of the lac operon include : the Z , Y , and A
genes containing the code for B - galactosidase , B - galactoside permease , and
B - galactoside transacetylase , respectively ; the regulatory gene ( i ) that codes ...
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
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 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 Microbiol microscopy mixture mutants needed 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