Bailey and Scott's Diagnostic Microbiology |
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Page 342
... slide . 2. Press another slide on top of it , squeeze the slides together , then pull them apart . This should result in two preparations of the proper thinness for staining and microscopy . 3. Label both slides and air dry and flame ...
... slide . 2. Press another slide on top of it , squeeze the slides together , then pull them apart . This should result in two preparations of the proper thinness for staining and microscopy . 3. Label both slides and air dry and flame ...
Page 567
... slide ( 50 by 75 mm or larger ) with the letters A , B , C , and G. The distance between the labels should be at least 20 mm . ( If 25- by 75 - mm slides are used , only two coagglutination reagents per slide should be tested . ) If the ...
... slide ( 50 by 75 mm or larger ) with the letters A , B , C , and G. The distance between the labels should be at least 20 mm . ( If 25- by 75 - mm slides are used , only two coagglutination reagents per slide should be tested . ) If the ...
Page 653
... slide , and allow it to run to the end . Allow to air dry . Do not fix . 4. Place the slide on staining rack , and flood with Solution A. Leave it for 4 minutes , and then rinse with distilled water . 5. Flood the slide with solution B ...
... slide , and allow it to run to the end . Allow to air dry . Do not fix . 4. Place the slide on staining rack , and flood with Solution A. Leave it for 4 minutes , and then rinse with distilled water . 5. Flood the slide with solution B ...
Contents
Microorganisms encountered in the eye 26 Grampositive nonsporeforming | 14 |
Methods of obtaining pure cultures | 17 |
Collection and transport of specimens | 31 |
Copyright | |
18 other sections not shown
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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