Pathological techniqueW.B. Saunders, 1897 - 387 pages |
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Page 82
... twenty - four hours the serum is removed by the aid of a clean pipette and brought to the laboratory . If the clot is in good condition , more serum will appear after another twenty - four hours , and if necessary this also may be used ...
... twenty - four hours the serum is removed by the aid of a clean pipette and brought to the laboratory . If the clot is in good condition , more serum will appear after another twenty - four hours , and if necessary this also may be used ...
Page 84
... twenty - four hours to determine whether they are sterile , after which they are ready for use . The blood - serum medium produced by this older method is especially suited for the cultivation of certain pathogenic bacteria —for ...
... twenty - four hours to determine whether they are sterile , after which they are ready for use . The blood - serum medium produced by this older method is especially suited for the cultivation of certain pathogenic bacteria —for ...
Page 97
... twenty - four hours , and on micro- scopic examination of cover - slip preparations of its blood and organs the characteristic encapsulated lanceolate diplo- cocci will be found ( see page 129 ) . The presence of the bacillus ...
... twenty - four hours , and on micro- scopic examination of cover - slip preparations of its blood and organs the characteristic encapsulated lanceolate diplo- cocci will be found ( see page 129 ) . The presence of the bacillus ...
Page 98
... twenty- four hours , are next to be studied , and the identity or diag- nosis of the bacteria whose colonies have grown out upon them is to be established . The identification of the infecting bacteria present in most cases may be made ...
... twenty- four hours , are next to be studied , and the identity or diag- nosis of the bacteria whose colonies have grown out upon them is to be established . The identification of the infecting bacteria present in most cases may be made ...
Page 102
... twenty - four hours . Solid culture - media , such as agar - agar , should be employed . Löffler's Method . - Treat the preparation for about one minute with the freshly filtered mordant solution , which is— Aqueous solution of tannic ...
... twenty - four hours . Solid culture - media , such as agar - agar , should be employed . Löffler's Method . - Treat the preparation for about one minute with the freshly filtered mordant solution , which is— Aqueous solution of tannic ...
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Other editions - View all
Pathological Technique: A Practical Manual for Workers in Pathological ... Frank Burr Mallory No preview available - 2016 |
Common terms and phrases
95 per cent absolute alcohol acetic acid acid fuchsin agar-agar alum alum-hematoxylin bacillus bacteria blood blood-serum blue bouillon Canada balsam carmine celloidin celloidin sections cells chlorid colonies color cover-glass preparations cover-slip culture-medium cultures Decolorize Dehydrate diagnosis differential stain dilute Diseases dissolved Distilled water drop eosin ether examination exudate fibrin filter-paper filtered fixing reagent formaldehyde gelatin gentian-violet glass glycerin grams granules heat hematoxylin hyaline hydrochloric acid imbedding incision incubator infected inoculation iodin knife lesions medium methylene-blue solution microscopic microtome mixture mounted Müller's fluid neuroglia-fibers nuclei obtained oil of cloves orcein organism osmic acid paraffin paraffin sections pathological picric acid pieces of tissue pipette placed plates potassium protoplasm reaction red corpuscles removed safranin saturated aqueous solution slide sodium solu specimens sputum Stain sections sterilized surface test-tubes thick tion tissue-elements tube twenty-four hours typhoid Unna's usually Wash in water Xylol Xylol balsam Zenker's fluid