Rapid Diagnostic Methods in Medical MicrobiologyCharles D. Graber Williams & Wilkins Company, 1970 - 343 pagine |
Dall'interno del libro
Risultati 1-3 di 25
Pagina 141
... sera to be tested . Adequate controls are in- cluded . The end point is hemolysis . If many sera are to be tested , a marked saving of time and materials is achieved by doing the procedure in a mi- crotiter system . The hemolytic test ...
... sera to be tested . Adequate controls are in- cluded . The end point is hemolysis . If many sera are to be tested , a marked saving of time and materials is achieved by doing the procedure in a mi- crotiter system . The hemolytic test ...
Pagina 257
... sera ( with known antigens ) and identifying HA positive viruses ( with known anti- sera ) . Unfortunately , not all human pathogenic viruses possess the HA property ( e.g. , polioviruses ) , and this limits the usefulness of the proce ...
... sera ( with known antigens ) and identifying HA positive viruses ( with known anti- sera ) . Unfortunately , not all human pathogenic viruses possess the HA property ( e.g. , polioviruses ) , and this limits the usefulness of the proce ...
Pagina 260
... sera ( acute and convalescent ) should be tested in order to show a significant ( 4 - fold or more ) rise in antibody titer . The sera are inactivated at 56 C for 30 minutes before testing . The procedure is the same as that described ...
... sera ( acute and convalescent ) should be tested in order to show a significant ( 4 - fold or more ) rise in antibody titer . The sera are inactivated at 56 C for 30 minutes before testing . The procedure is the same as that described ...
Sommario
SYLVIA G CARY M S Department of Bacterial Diseases Walter Reed | 3 |
JAMES B GROGAN PH D Departments of Surgery and Microbiology | 4 |
Identification in Cultures of Blood and Body | 12 |
Copyright | |
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Parole e frasi comuni
acid agar plates agent agglutination Amer anaerobic animal anthracis antibiotics antigen antisera bacilli Bact bacteria bile biochemical blood agar bottles broth Brucella buffered carbohydrates catalase cell cultures centrifuge characteristic chick embryos Clin clinical specimens coagulase colonies color concentration containing detection dextrose diagnosis Difco differentiation dilution disease disk Enterobacteriaceae ferment filter fluid fluorescent antibody forms genus glucose Gram negative Gram positive Group grow growth medium hemolysis hemolytic human identification incubation infection inhibition inoculated inoculum kidney laboratory lactose leptospires leptospirosis metabolic method mice Microbiol microorganisms Microscopic examination minutes motile mycoplasma Neisseria nitrate organisms Pasteurella pathogenic penicillin pipette pneumococci prepared primary isolation Proc procedure produce pseudomonads rapid reactions reagent saline solution Salmonella sensitivity sensitivity test sera serologic serum Shigella slide smears species sputum staphylococci sterile strains streptococci substrate sucrose suspension swabs technique temperature tion tissue titer tube cultures usually viral virulent virus viruses