Hydatid disease in Northern Sweden. An orientation of hydatid disease in Northern Sweden and an evaluation of the Casoni and complement fixation tests.
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Adolescent↗
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Results for “Complement Fixation Tests”
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Antigenic relationships among strains of Mycoplasma mycoides var. mycoides, M. capri and M. laidlawii revealed by complement-fixation tests.
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Animals↗
Complement fixation test for pneumocytosis.
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Adult↗
[Studies on the demonstration of serologic differences between the group antigens from various adenovirus types. II. Demonstration of antigen differences with the complement fixation test in the isofixation technic].
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Adenoviridae↗
[Antigen components of the poliovirus in the complement fixation test].
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Antigen-Antibody Reactions↗
[Determination of the antigenic dilution concentration in the complement fixation test].
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Animals↗
[Significance of soluble and insoluble antigens in complement fixation tests for the diagnosis of toxoplasmosis].
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Antigens↗
[Method of adaptation of the Kolmer values in determination of hemolysin with the complement fixation test in virus diseases. Practical note].
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Complement Fixation Tests↗
Preparation of toxoplasma antigen for use in the complement-fixation test.
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Animals↗
[The value of the complement fixation test in the laboratory diagnosis of toxoplasmosis].
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Complement Fixation Tests↗
Serological survey of anaplasmosis incidence in East Africa, using the complement-fixation test.
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Anaplasma↗
Determination of anti-insulin activity by means of the complement fixation test.
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Adolescent↗
The diagnostic value of a gonococcal complement fixation test.
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Antigens, Bacterial↗
A preliminary study of the serotypes of Corynebacterium genitalium by means of the complement-fixation test.
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Animals↗
Antibody estimation by indirect complement fixation test for foot-and-mouth disease in cattle.
Antibody against foot-and-mouth disease (FMD) virus was measured by the indirect complement fixation (ICF) test. For this test serum samples were collected from cattle experimentally infected with FMD virus of O, A and Asia 1 types, as well as cattle infected in the field. Two types of antigen were used. One was antigen derived from infected lingual epithelial culture prepared by Frenkel's method with each type of the virus. The other was antigen derived from the lingual epithelium of cattle infected by virus inoculation. ICF antibody began to be dectected about 4 5 days after inoculation. It reached a maximum titer 10 14 days after inoculation, remaining at this titer for about a week or two, and then decreased gradually. It was, however, detectable even 63 days after inoculation. The rise and fall of ICF antibody was parallel with that of neutralizing antibody, although that antibody was always lower in titer than this. ICF antibody was detected type-specifically from cattle infected experimentally and naturally. These results indicated that the ICF test was available for the routine serological diagnosis and epizootiological investigation and research.
Animals↗
[Evaluation and introduction of the indirect immunofluorescence test (toxoplasmosis) in the diagnostic services of the Pedro Kourí Institute of Tropical Medicine and its relation to the complement fixation test].
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Adolescent↗
A complement-fixation test for the bovine leukemia (C-type) virus.
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Animals↗
Complement fixation test for the diagnosis of Lyme disease.
Sera from 43 patients were tested for complement-fixing antibodies to Borrelia burgdorferi; these patients included 8 with confirmed Lyme disease, 21 who were serologically positive but not likely to have Lyme disease, and 14 who were serologically negative. Seven individuals, all confirmed Lyme disease patients, had complement-fixing antibodies. Complement fixation may be a useful confirmatory test for Lyme disease.
Antibodies, Bacterial↗