Manual of Clinical MicrobiologyEdwin H. Lennette, American Society for Microbiology |
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Page 481
... serum or in broth with 50 % serum added to attempt to mimic the in vivo situation . Since serum itself is a variable product , samples from a large number of healthy individuals should be pooled . Differ- ent batches of normal serum may ...
... serum or in broth with 50 % serum added to attempt to mimic the in vivo situation . Since serum itself is a variable product , samples from a large number of healthy individuals should be pooled . Differ- ent batches of normal serum may ...
Page 737
... serum and no reaction with the negative serum is consid- ered optimal . Test procedure . Inactivate the serum specimens for 30 min at 56 ° C . Prepare serial dilutions of the serum in 1 % NRS as follows : 1. Into microtitration U plates ...
... serum and no reaction with the negative serum is consid- ered optimal . Test procedure . Inactivate the serum specimens for 30 min at 56 ° C . Prepare serial dilutions of the serum in 1 % NRS as follows : 1. Into microtitration U plates ...
Page 804
... serum are likely to contain antibodies to certain simian viruses , and if the viral isolates are recovered in monkey kidney cells , the conjugates may give positive staining with cells containing the simian viruses as contaminants ...
... serum are likely to contain antibodies to certain simian viruses , and if the viral isolates are recovered in monkey kidney cells , the conjugates may give positive staining with cells containing the simian viruses as contaminants ...
Contents
Indigenous and Pathogenic Microorganisms of Humans | 25 |
Collection Handling and Processing of Specimens HENRY D ISENBERG JOHN | 52 |
Streptococci and Aerococci | 83 |
Copyright | |
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abscesses acid aerobic aeruginosa agar plate agents agglutination anaerobic antibiotics antibody antigen antimicrobic antisera assay aureus bacilli bacteria biochemical biotypes blood agar broth carbohydrates catalase cause cells Center for Disease Chapter characteristics Clin clinical specimens cocci coli colonies conidia containing cultures decarboxylase detection diagnosis diameter differentiated dilution disk Enterobacteriaceae Esculin examination fermentation flagella fluid fluorescence fungi gentamicin genus glucose Gram stain gram-negative gram-positive grow growth hemolysis human hyphae identification incubation indole infections inhibition inoculated inoculum isolated laboratory lactose lesions maltose medium method Microbiol Microbiology microorganisms microscope morphology Motility mycobacteria negative Neisseria nitrate organisms oxidase pathogenic patients penicillin pigment positive prepared procedures produce Pseudomonas reactions reagents Salmonella sample serological serotypes serum skin slide smears species sputum Staphylococcus sterile strains streptococci subculture susceptibility testing swab Table technique temperature tion tissue titer tive tract treponemal tube urease urine usually Vibrio Xylose yeast µg/ml