Manual of Methods for General Bacteriology |
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Page 80
In addipounds has been discussed in the preceding par- tion to chelating agents already mentioned , agraphs . Most bacteria so far studied utilize many medium components ( amino acids , citrate , ammonia for the synthesis of the ...
In addipounds has been discussed in the preceding par- tion to chelating agents already mentioned , agraphs . Most bacteria so far studied utilize many medium components ( amino acids , citrate , ammonia for the synthesis of the ...
Page 95
Compositions of undefined ( A ) and semidefined ( B ) media 51 through 63 for the bacteria listed in Table 1 Amt ( in units given in column 1 ) / liter for medium : Component 51B 52A53A 54A55A " 56A 57A 58A ' 59A " 60A " 61A62A 63A ...
Compositions of undefined ( A ) and semidefined ( B ) media 51 through 63 for the bacteria listed in Table 1 Amt ( in units given in column 1 ) / liter for medium : Component 51B 52A53A 54A55A " 56A 57A 58A ' 59A " 60A " 61A62A 63A ...
Page 103
7.0 7.0 6.8 d Amt ( in units given in column 1 ) / liter for medium : Component 54C 55C 56C 570 58C 59C ' 60C * 61C 62C 63C 64B 65C 66C ' Glucose ” ( g ) 10 25 10 10 30 30 2.5 " 10.4 2.0 10 10 10 Sodium acetate ( g ) 10 10 5.0 10 6.0 ...
7.0 7.0 6.8 d Amt ( in units given in column 1 ) / liter for medium : Component 54C 55C 56C 570 58C 59C ' 60C * 61C 62C 63C 64B 65C 66C ' Glucose ” ( g ) 10 25 10 10 30 30 2.5 " 10.4 2.0 10 10 10 Sodium acetate ( g ) 10 10 5.0 10 6.0 ...
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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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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