Titlebook: Immunology in Plant Sciences; Hans-Ferdinand Linskens,John F. Jackson Book 1986 Springer-Verlag Berlin Heidelberg 1986 biology.immunology.

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Immunodetection of Phytochrome: Immunocytochemistry, Immunoblotting, and Immunoquantitation,e quickly becoming indispensible for many purposes, including one-step purification of antigens, their visualization in situ by immunocytochemistry and on nitrocellulose blots of polyacrylamide gels, and their quantitation by radioimmunoassay or enzyme immunoassay. The relatively recent development

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The Measurement of Low-Molecular-Weight, Non-Immunogenic Compounds by Immunoassay,not themselves stimulate antibody formation. In order to produce the required antibodies, the small molecule (the hapten) must be covalently linked to a larger molecule (usually a protein) that is immunogenic and this conjugate used to immunise an animal. The antiserum thus generated will contain a

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Radioimmunoassay and Western Blot Analysis of Acyl Carrier Protein Isoforms in Plants,s and subsequent elongation and desaturation reactions in plants (Stumpf 1980). In yeast and animals, ACP is an integral part of the multifunctional polypeptide, fatty acid synthase, but in bacteria and plants, ACP is a separate, small polypeptide (ca. 9 kDa MW) which is acidic and heat stable (Maje

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Immunofluorescent Labelling of Enzymes,requisite for understanding cellular metabolism. One of the most sensitive and specific techniques for reaching this goal is the in situ localization of enzymes by immunological methods. In principle the specificity of the antigen(enzyme)-antibody reaction is combined with a labelling technique whic

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Quantitative Immunochemistry of Plant Phosphoenolpyruvate Carboxylases,entists. The enzyme catalyses the reaction of CO.H. and phosphoenolpyruvate to produce oxaloacetate, immediately reduced to form malate; this latter can be oxidatively decarboxylated by NADP malic enzyme, and thus, appears to be a physiological vector for carbon (CO.) and energy (reducing power). Ex

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