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Enzyme-Linked Immunosorbant Assay (ELBA)
2003In general, immunological methods are not very well suited for a quantitative determination of the antigen to be studied. The ELISA technique, however, can be used for a quantitative or at least semiquantitative determination of the concentration of a certain antigen. The method was first introduced by Engvall and Perlmann (1).
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Competitive Enzyme-Linked Immunosorbent Assay
2005Competitive enzyme-linked immunosorbent assay provides an alternative to dual-antibody sandwich enzyme-linked immunosorbent assay and is widely used for the measurement of substances in biological liquids.
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American Journal of Tropical Medicine and Hygiene, 1984
A double antibody micro enzyme-linked immunosorbent assay (ELISA) for identifying Plasmodium falciparum sporozoites in mosquitoes is described. Using monoclonal antibodies made against South American P.
T. Burkot, J. Williams, I. Schneider
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A double antibody micro enzyme-linked immunosorbent assay (ELISA) for identifying Plasmodium falciparum sporozoites in mosquitoes is described. Using monoclonal antibodies made against South American P.
T. Burkot, J. Williams, I. Schneider
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Development of an enzyme-linked immunosorbent assay for podophyllotoxin
International Immunopharmacology, 2005A competitive indirect enzyme-linked immunosorbent assay (ciELISA) for podophyllotoxin was developed by using polyclonal antibody, and its suitability for the determination of this analyte in spiked water samples was studied. To avoid antibody production to the linker, the succinoyl-podophyllotoxin (hapten) mimicking the analyte was synthesized and ...
Xing Zhang +7 more
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An Enzyme-Linked Immunosorbent Assay for Calmodulin
1985Calmodulin (CaM) is a Ca2+-binding protein notably important in the translation of Ca2+ signals inside the cell (as reviewed [1, 2]) [cf. A.R. Means & J.G. Chafouleas, Vol. 13, #A-7, this series — Ed.]. It is found throughout the plant and animal kingdoms and its sequence is highly conserved [3].
I. R. Cottingham +2 more
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Journal of medical entomology, 1988
A direct enzyme-linked immunosorbent assay (ELISA) was developed for bloodmeal identification of seven hosts. Commercially available reagents are used; the test can be completed in only 4.5 h.
John C. Beier +6 more
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A direct enzyme-linked immunosorbent assay (ELISA) was developed for bloodmeal identification of seven hosts. Commercially available reagents are used; the test can be completed in only 4.5 h.
John C. Beier +6 more
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Cascade enzyme-linked immunosorbent assay (CELISA)
Biosensors and Bioelectronics, 2009Immunoassays are representative biochemical detection methods. Among them, sandwich-type immunoassays, typified by sandwich ELISA, have used in disease diagnosis or biochemical detection with high target selectivity. Horseradish peroxidase and alkaline phosphatase have been typically used for signal amplification in ELISA.
Bong Hyun Chung +6 more
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To Perform Enzyme-Linked Immunosorbent Assay
2018Enzyme-linked immunosorbent assay (ELISA) is an immunoassay that combines the specificity of antibody and antigen usually detected in presence of enzyme conjugated with antibody. The enzyme linked with the antibody reacts with specific substrate to produce colored product which is related to antigen or antibody concentration.
Vijay Kumar, Kiran Dip Gill
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An enzyme-linked immunosorbent assay for the quantitation of DNA
Journal of Immunological Methods, 1989Description d'une methode de dosage de l'ADN par ELISA dans laquelle l'ADN, apres application des echantillons sur les microplaques de titration, est modifie chimiquement par le metabisulphite de sodium et la O-methylhydroxylamine.
John W. McAvoy, N.A. Richardson
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Enzyme-linked immunosorbent assay (ELISA). Quantitative assay of immunoglobulin G.
Immunochemistry, 1971E. Engvall, P. Perlmann
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