Results 311 to 320 of about 422,292 (362)
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Stabilization of Fluorescence in Preparates treated by the Fluorescent Antibody Technique
Nature, 1966WITH the fluorescent antibody technique it is often difficult to see results; it is especially difficult to prepare good photomicrographs of positive structures with low fluorescence intensity. Short-term illumination of sections with concentrated ultra-violet and blue light causes the fluorescence intensity of fluorescein isothiocyanate (FITC) to ...
M. Mrenová, P. Albrecht
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Avian Diseases, 1972
Attempts (1,2,4,5) have been made to develop more rapid and accurate methods of detecting avian encephalomyelitis (AE) antibody in chickens in place of the virus-neutralization test (VNT) and embryo-susceptibility test. A fluorescent antibody blocking test (FABT) was recently reported by Davis and Lukert (1).
Won-Pil Choi, Shiro Miura
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Attempts (1,2,4,5) have been made to develop more rapid and accurate methods of detecting avian encephalomyelitis (AE) antibody in chickens in place of the virus-neutralization test (VNT) and embryo-susceptibility test. A fluorescent antibody blocking test (FABT) was recently reported by Davis and Lukert (1).
Won-Pil Choi, Shiro Miura
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SALMONELLAE AND THE FLUORESCENT-ANTIBODY TECHNIQUE: A CURRENT EVALUATION1
Journal of Milk and Food Technology, 1969The increased microbiological surveillance of foods by government regulatory agencies and industry has shown that salmonellae are an important cause of food-borne disease. The significance of salmonellae in food-borne disease has made it mandatory for regulatory agencies as well as industry to develop a rapid, reliable, and reproducible method for the ...
J. M. Goepfert, N. F. Insalata
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Fluorescent Antibody Technique for Cryptococcus
JAMA: The Journal of the American Medical Association, 1974To the Editor.— In the Nov 19,1973, issue ofThe Journal(226:1009, 1973), Dr. Paul Wolf of Stanford University had a letter published purporting to describe a new method to identify cryptococcal infection. In all fairness to Dr. R. A. Vogel, you should be aware that he reported this method initially in 1958 and again in 1961 and 1966.
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DIAGNOSIS OF TULAREMIA BY FLUORESCENT-ANTIBODY TECHNIQUES [PDF]
, 1964 Abstract : P. tularensis, the causative organism of tularemia, can be readily and positively identified in formalin-fixed and paraffin-embedded human tissues. This was done in eight of nine cases examined. The diagnostic and therapeutic implications of this advance are discussed.
John D. White, Malcolm H. McGavran
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Fluorescent Antibody Techniques
American Journal of Diseases of Children, 1961The diagnosis of early, mild, or atypical whooping cough is dependent upon identification of the etiologic agent. Although procedures for the isolation of Bordetella pertussis 1 have been available for many years and are of proven diagnostic aid, they have not gained the wide usage they seem to deserve.
Pearl L. Kendrick +2 more
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Antibody Production in Human Malaria as Determined by the Fluorescent Antibody Technique
Science, 1962No reliable serological test has been available in the past to follow the course of antibody production in malarial infections. The indirect method of immunofluorescence was utilized in this investigation to study antibody response to sporozoite-induced Plasmodium vivax infections in two human volunteers.
Peter G. Contacos +4 more
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Identification of fungi by the fluorescent antibody technique [PDF]
, 1972 The fluorescent antibody technique was investigated as a means of facilitating the recognition and identification of the fungal components of a western red cedar (Thuja plicata Donn) heartwood flora in situ. Fungi isolated from the heartwood were grown in bulk and prepared for two different injection trials. In one trial the antigen was the particulate
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Intrahepatic Localisation of Australia Antigen by Fluorescent Antibody Technique
Vox Sanguinis, 1973Abstract. Our results give further support to the suggestion that the various patterns of intrahepatic localisation of Australia antigen represent different stages of intracellular accumulation of Australia antigen rather than technical differences or differences in the specificity of antibody to Australia antigen.
R. Müller, J. Maess
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