Results 181 to 190 of about 9,412,541 (217)
RAPID IMMUNOENZYME MOHS TECHNIQUE FOR SKIN CANCER REMOVAL
Christopher B. Zachary, William Perkins
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Analytical Biochemistry, 1973
Abstract Conditions have been established for estimating antibody potency by conducting an antigen-antibody reaction whose product is soluble and where the antigen is an enzyme whose activity is reduced on combination with antibody. The antigen preparations were made from placental alkaline phosphatase, and antisera from rabbits were collected.
Sidney Green +4 more
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Abstract Conditions have been established for estimating antibody potency by conducting an antigen-antibody reaction whose product is soluble and where the antigen is an enzyme whose activity is reduced on combination with antibody. The antigen preparations were made from placental alkaline phosphatase, and antisera from rabbits were collected.
Sidney Green +4 more
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A Rapid Immunoenzyme Double Labeling Technique Using EPOS Reagents
Journal of Histotechnology, 1995AbstractWe present a rapid method for a double immunoenzyme staining of formalin fixed, paraffin embedded tissue sections using antibodies labeled with a peroxidase enzyme polymer system (EPOS) recently introduced by Dako. This method is rapid, taking less than 3 hr, is virtually background free, and has a sensitivity comparable to the more cumbersome ...
Joan Miller +4 more
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[48] Immunoenzymic techniques for biomedical analysis
1976Publisher Summary This chapter discusses the immunoenzymic techniques for biomedical analysis. Since the first publications on the preparation and uses of enzyme labeled proteins appeared, there has been continuous development in this area. An appreciable number of immunoenzymic techniques, which make use of enzymes coupled to antigens or antibodies,
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M, Lin Chu, R B, Marshall
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Immunohistochemical studies on human gastric mucosa
Virchows Archiv A Pathological Anatomy and Histology, 1978Two different fixatives were applied to human gastric mucosa for the study of antigenic marker substances. The first consists of 96% ethanol and 1% acetic acid (EA method), the second of 4% formaldehyde, 0.5% picric acid and 0.25% glutaraldehyde (FPG method).
W. Rapp, K. Wurster, W. D. Kuhlmann
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Journal of Immunological Methods, 1993
A method for detecting granulocyte-macrophage colony-stimulating factor (GM-CSF) receptors has been devised using human macrophages and a GM-CSF/IL-3-dependent human megakaryoblastic leukemia cell line (M-07e). Recognition of the factor-binding site was accomplished by linking recombinant human (rh) unglycosylated GM-CSF previously labeled with ...
Roncaroli F +6 more
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A method for detecting granulocyte-macrophage colony-stimulating factor (GM-CSF) receptors has been devised using human macrophages and a GM-CSF/IL-3-dependent human megakaryoblastic leukemia cell line (M-07e). Recognition of the factor-binding site was accomplished by linking recombinant human (rh) unglycosylated GM-CSF previously labeled with ...
Roncaroli F +6 more
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[Evaluation of an immunoenzyme technique for the diagnosis of syphilis].
Enfermedades infecciosas y microbiologia clinica, 1991A comparative study of an enzyme immunoassay (EIA Captia Syphilis Mercia), FTA-Abs and VDRL to detect anti-Treponema pallidum antibodies was carried out in overall 290 subjects: 113 had a diagnosis of syphilis (40 primary and 73 secondary) and 117 were controls (40 with nonsyphilitic ulcers, 52 with falsely positive VDRL and 85 healthy subjects).
M V, Borobio, J M, Ruiz, E J, Perea
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Abo-grouping of human hair by immunoenzyme technique
Forensic Science International, 1987L. Pötsch-Schneider, L. Penzes
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