Results 201 to 210 of about 19,840 (238)
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1996
Rocket immunoelectrophoresis (also referred to as electroimmunoassay) is a simple, quick, and reproducible method for determining the concentration of a specific protein in a protein mixture. The method, originally introduced by Laurell (1) involves a comparison of the sample of unknown concentration with a series of dilutions of a known concentration ...
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Rocket immunoelectrophoresis (also referred to as electroimmunoassay) is a simple, quick, and reproducible method for determining the concentration of a specific protein in a protein mixture. The method, originally introduced by Laurell (1) involves a comparison of the sample of unknown concentration with a series of dilutions of a known concentration ...
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Scandinavian Journal of Immunology, 1973
Synonym— Laurell antigen‐antibody crossed electrophoresis (82) ad modum Clarke & Freeman (29).
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Synonym— Laurell antigen‐antibody crossed electrophoresis (82) ad modum Clarke & Freeman (29).
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Quantitation of antigens by immunoelectrophoresis
Immunochemistry, 1974Abstract An immunoelectrophoretic method has been described for the quantitation of 4 or 5 proteins simultaneously. The method is useful for monitoring complex antigen mixtures provided proper antigen standards are employed and the antiserum is of adequate titer. Monospecific antiserum is not required for the quantitative assay.
Raymond N. Hiramoto, Vithal K. Ghanta
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Starch-Gel Immunoelectrophoresis,
The Journal of Immunology, 1959Summary An immunoelectrophoretic method based upon one-dimensional and two-dimensional zone electrophoresis is described in detail. A discontinuous system of buffers was used in order to increase the resolving power of the starch-gel electrophoresis and to increase the sensitivity of the antigen-antibody reactions in agar gel.
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2003
Ressler first described in 1960 (1) a form of immunoelectrophoresis now called crossed immunoelectrophoresis (CIE) or two-dimensional immunoelectrophoresis, which was later improved by Laurell (2), Clarke and Freeman (3), and Weeke (4), among others.
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Ressler first described in 1960 (1) a form of immunoelectrophoresis now called crossed immunoelectrophoresis (CIE) or two-dimensional immunoelectrophoresis, which was later improved by Laurell (2), Clarke and Freeman (3), and Weeke (4), among others.
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Primer of Immunoelectrophoresis
Archives of Dermatology, 1971This book provides a brief introduction to the theory and principles of immunoelectrophoresis. A chapter each is provided for identification of major proteins in human serum and some of the more illustrative pathologic sera. The detail given to the specifications of the electrophoresis cell, and preparation of the troughs and wells in the agar seems ...
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Shape of the Precipitate in Immunoelectrophoresis
Nature, 1960IN immunoelectrophoresis, according to Grabar and Williams1, diffusion of the electrophoretically separated antigens towards the immune serum added in longitudinal basins parallel to the migration axis after the electrophoretic separation will result in the formation of precipitates in the gel, occupying varying positions between antigen and antibody ...
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Improved agarose for immunoelectrophoresis
Analytical Biochemistry, 1976Abstract Alkali-treatment of agarose was found to be a very simple method to produce charge-free agarose from commercially available agarose in high yield (about 90%) with highly reduced content of sulphate groups and very low electroendosmotic flow. Applications of the agarose in immunoelectrophoretic experiments are also described.
Bo Lönnerdal, Torgny Låås
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Immunoelectrophoresis of Cataractous Lenses
Archives of Ophthalmology, 1959The history of immunology of lens proteins goes back to Uhlenhuth, 1 who 55 years ago showed by precipitation tests the organ specificity of some of the lens components. This was verified later by Burky, Woods, and Woodhall. 2 They found that mainly the so-called α-crystallin was organspecific.
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Immunoelectrophoresis of the proteins of the corneal epithelium
Experimental Eye Research, 1963The proteins of the corneal epithelium are separated into a greater number of fractions by high-tension agar electrophoresis than by paper electrophoresis. The distribution of the different fractions is greatly influenced by the ionic strength of the buffer solution.
M. Rabaey, Jules François
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