Manual of Methods for General Bacteriology |
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Page 444
448 A numerical taxonomy study involves five essential steps : ( i ) selection of
strains , ( ii ) selection of tests , ( iii ) coding and arraying of test results in a format
suitable for analysis by a computer , ( iv ) computer analysis of the relationships ...
448 A numerical taxonomy study involves five essential steps : ( i ) selection of
strains , ( ii ) selection of tests , ( iii ) coding and arraying of test results in a format
suitable for analysis by a computer , ( iv ) computer analysis of the relationships ...
Page 445
DATA CODING 445 as additional strains whose identity has been established ( “
reference strains ” ) for comparative purposes . Type and reference strains can be
obtained from culture collections such as the American Type Culture Collection ...
DATA CODING 445 as additional strains whose identity has been established ( “
reference strains ” ) for comparative purposes . Type and reference strains can be
obtained from culture collections such as the American Type Culture Collection ...
Page 447
Although the merits of both equations have been adequately discussed
elsewhere ( 4 , 5 ) , it needs to be emphasized that the Ssm coefficient reflects the
presence of a large number of nega - tive attributes between strains , thereby
giving an ...
Although the merits of both equations have been adequately discussed
elsewhere ( 4 , 5 ) , it needs to be emphasized that the Ssm coefficient reflects the
presence of a large number of nega - tive attributes between strains , thereby
giving an ...
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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