Manual of Methods for General Bacteriology |
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Page 231
After 2 or 3 reversión promoted by several commonly used days of incubation at
37°C , determine the relachemical ... revertants from partial revertants or
suppressed and NTG , which has a specificity spectrum simstrains by
determining ...
After 2 or 3 reversión promoted by several commonly used days of incubation at
37°C , determine the relachemical ... revertants from partial revertants or
suppressed and NTG , which has a specificity spectrum simstrains by
determining ...
Page 267
After very able so that one must directly examine a bacte - gentle swirling to mix
the contents thoroughly , rium to determine its plasmid content . Such an place
the tube in ice for 20 min . analysis usually can be performed to determine 6 .
After very able so that one must directly examine a bacte - gentle swirling to mix
the contents thoroughly , rium to determine its plasmid content . Such an place
the tube in ice for 20 min . analysis usually can be performed to determine 6 .
Page 315
Once this has been determined , the lower discriminator is set to exclude most of
the background ( i . e . , set at 10 ) and the ... However , at very low count rates it
may be necessary to determine the effect of sample quench by counting an ...
Once this has been determined , the lower discriminator is set to exclude most of
the background ( i . e . , set at 10 ) and the ... However , at very low count rates it
may be necessary to determine the effect of sample quench by counting an ...
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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