Manual of Methods for General Bacteriology |
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Page 79
Key to Media for Representative Bacteria .2 . Undefined and Semidefined Media .3 . Defined Media 7.3 . QUANTITATIVE GROWTH - RESPONSE ASSAYS 7.3.1 . Amino Acids ( Arginine ) .2 . Vitamins 7.4 . LITERATURE CITED 80 80 80 80 82 83 83 83 ...
Key to Media for Representative Bacteria .2 . Undefined and Semidefined Media .3 . Defined Media 7.3 . QUANTITATIVE GROWTH - RESPONSE ASSAYS 7.3.1 . Amino Acids ( Arginine ) .2 . Vitamins 7.4 . LITERATURE CITED 80 80 80 80 82 83 83 83 ...
Page 407
Systematics in bacteriology is concerned with three interrelated topics : ( i ) classification , the arranging of bacteria with similar phenotypic or genetic characteristics into groups ; ( ii ) nomenclature , the naming of bacteria ...
Systematics in bacteriology is concerned with three interrelated topics : ( i ) classification , the arranging of bacteria with similar phenotypic or genetic characteristics into groups ; ( ii ) nomenclature , the naming of bacteria ...
Page 513
... 438 Deoxyribonucleic acid ( see also Nucleic acids ) determination in bacteria , 348-349 , 350 determination of moles percent guanine plus cytosine , 457-458 diphenylamine assay for , 456-457 isolation and quantitation , 244-245 ...
... 438 Deoxyribonucleic acid ( see also Nucleic acids ) determination in bacteria , 348-349 , 350 determination of moles percent guanine plus cytosine , 457-458 diphenylamine assay for , 456-457 isolation and quantitation , 244-245 ...
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Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
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Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York