Manual of Methods for General Bacteriology |
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Page 306
... to calculate the equilibrium constant or stoichiometry of binding , respectively (
41 ) ( Fig . 7 ) . This can be determined by incubation of the macromolecule and
ligand , followed by gel filtration on Sephadex G - 50 which has been equilibrated
...
... to calculate the equilibrium constant or stoichiometry of binding , respectively (
41 ) ( Fig . 7 ) . This can be determined by incubation of the macromolecule and
ligand , followed by gel filtration on Sephadex G - 50 which has been equilibrated
...
Page 318
... and Ro are the total rates and the from the mean . background rate ,
respectively , and t , and to are There are a number of different kinds of error : the
times for R , and Rs . i.e. , probable error , where the true value is likely to exceed
the error ...
... and Ro are the total rates and the from the mean . background rate ,
respectively , and t , and to are There are a number of different kinds of error : the
times for R , and Rs . i.e. , probable error , where the true value is likely to exceed
the error ...
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
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