Manual of Methods for General Bacteriology |
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Page 59
When very has entered the separation gel , at which point it long gels are not
required , electrophoresis , fixing is increased to 145 V for the remainder of the
and staining , and drying can all be accomplished run . For best resolution , the
gel ...
When very has entered the separation gel , at which point it long gels are not
required , electrophoresis , fixing is increased to 145 V for the remainder of the
and staining , and drying can all be accomplished run . For best resolution , the
gel ...
Page 296
In this way , any number of common and while other ions are not sorbed or are
retained . trace inorganic elements as well as radionuclides Fractionation is the
process of separating several and trace organic compounds have been ...
In this way , any number of common and while other ions are not sorbed or are
retained . trace inorganic elements as well as radionuclides Fractionation is the
process of separating several and trace organic compounds have been ...
Page 325
Thus , separation is Methyl red ( 0 . 5 ppm ) can be added to the ... For
preparative - scale separations , is to base the separation on two strategies , i . e .
, a commercial or homemade device can be used . size and pl . Thus , a sample
may first ...
Thus , separation is Methyl red ( 0 . 5 ppm ) can be added to the ... For
preparative - scale separations , is to base the separation on two strategies , i . e .
, a commercial or homemade device can be used . size and pl . Thus , a sample
may first ...
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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