Manual of Methods for General Bacteriology |
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Page 318
... are the total rates and the background rate , respectively , and te and to are the
times for R , and Rh . 16 . 5 . GEL ELECTROPHORESIS times required for
counting background and for total count with a given standard error , limits of
detection ...
... are the total rates and the background rate , respectively , and te and to are the
times for R , and Rh . 16 . 5 . GEL ELECTROPHORESIS times required for
counting background and for total count with a given standard error , limits of
detection ...
Page 366
... and triphosphate , respectively ; F6P , fructose - 6 - phosphate ; FDP , fructose -
1 , 6 - diphosphate ; G6P , glucose - 6 ... respectively ; EDTA ,
ethylenediaminetetraacetic acid ; NAD and NADH , oxidized and reduced
nicotinamide adenine ...
... and triphosphate , respectively ; F6P , fructose - 6 - phosphate ; FDP , fructose -
1 , 6 - diphosphate ; G6P , glucose - 6 ... respectively ; EDTA ,
ethylenediaminetetraacetic acid ; NAD and NADH , oxidized and reduced
nicotinamide adenine ...
Page 383
Components involved in transcription of the ląc 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 ląc 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
55 | 32 |
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 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 enrichment 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 mg/liter microscopy mixture mutants 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