Bailey and Scott's Diagnostic MicrobiologyMosby, 1982 - 705 pagine |
Dall'interno del libro
Risultati 1-3 di 59
Pagina 467
... minutes before preparing the slides . With an applicator stick apply some of the stool material from the paper towel to two slides and let them dry for several hours at 37 C or overnight at room tem- perature . The PVA - stool mixture ...
... minutes before preparing the slides . With an applicator stick apply some of the stool material from the paper towel to two slides and let them dry for several hours at 37 C or overnight at room tem- perature . The PVA - stool mixture ...
Pagina 468
... minutes . 4. Place in 70 % ethyl alcohol for 5 minutes . * 5. Wash in running tap water for 10 minutes . 6. Place in working solution of iron - hema- toxylin staining solution for 4 to 5 minutes . 7. Wash in running tap water for 10 ...
... minutes . 4. Place in 70 % ethyl alcohol for 5 minutes . * 5. Wash in running tap water for 10 minutes . 6. Place in working solution of iron - hema- toxylin staining solution for 4 to 5 minutes . 7. Wash in running tap water for 10 ...
Pagina 469
... minutes . 3. Place in 50 % ethyl alcohol for 3 minutes . 4. Wash in running tap water for 3 minutes . 5. Place in 4 % ferric ammonium sulfate mordant for 5 minutes . 6. Wash in tap water for 1 minute . 7. Place in 0.5 % aqueous ...
... minutes . 3. Place in 50 % ethyl alcohol for 3 minutes . 4. Wash in running tap water for 3 minutes . 5. Place in 4 % ferric ammonium sulfate mordant for 5 minutes . 6. Wash in tap water for 1 minute . 7. Place in 0.5 % aqueous ...
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