Bailey and Scott's Diagnostic MicrobiologyMosby, 1982 - 705 pagine |
Dall'interno del libro
Risultati 1-3 di 68
Pagina 620
... prepared . One or two plates per 100- to 200 - ml batch should be incubated at 35 C overnight to deter- mine sterility and later discarded . Thayer - Martin agar ( see p . 643 ) for the selec- tive isolation of Neisseria gonorrhoeae and ...
... prepared . One or two plates per 100- to 200 - ml batch should be incubated at 35 C overnight to deter- mine sterility and later discarded . Thayer - Martin agar ( see p . 643 ) for the selec- tive isolation of Neisseria gonorrhoeae and ...
Pagina 645
... prepared fresh each time the medium is prepared . The cystine may be dis- solved in 6 ml of 0.1 N HCl and added sep- arately , in which case it may be necessary to add 6 ml of 0.1 N NaOH to make sure that the final pH is correct . Todd ...
... prepared fresh each time the medium is prepared . The cystine may be dis- solved in 6 ml of 0.1 N HCl and added sep- arately , in which case it may be necessary to add 6 ml of 0.1 N NaOH to make sure that the final pH is correct . Todd ...
Pagina 676
... prepared and inoculated immediately . Urease test broth is prepared according to the formula of Rustigian and Stuart.9.10 It may be used for identification of bacteria on the basis of urea utilization and is particularly recommend- ed ...
... prepared and inoculated immediately . Urease test broth is prepared according to the formula of Rustigian and Stuart.9.10 It may be used for identification of bacteria on the basis of urea utilization and is particularly recommend- ed ...
Sommario
Microorganisms encountered in the eye 26 Grampositive nonsporeforming | 14 |
Methods of obtaining pure cultures | 17 |
Collection and transport of specimens | 31 |
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Parole e frasi comuni
acid activity addition agar agar plate agents agglutination amounts anaerobic antibiotics antibody antigen antimicrobial appear bacilli bacterial blood agar blood culture bottle broth caused cells Chapter characteristics Clin clinical collection colonies concentration containing described detection determined develop diagnosis differentiation dilution direct disease disk Distilled water drugs effective eggs examined fluid forms frequently genus glucose Gram gram-negative grow growth human identification important incubation indicated infection inoculated involved isolation laboratory less material medium meningitis method Microbiol Microbiology minutes mixed negative noted obtained occur organisms pathogenic patients placed plate pneumonia positive prepared present procedure produce rapid reaction reagents recommended reference reported resistant Salmonella selective serum slant slide smears sodium solution species specimens sputum stain sterile streptococci swab Table technique tion tissue tract tube urine usually various