Titlebook: Membrane Proteins; A Laboratory Manual Angelo Azzi,Urs Brodbeck,Peter Zahler Book 1981 Springer-Verlag Berlin Heidelberg 1981 ATP.Biomembra

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G. Brandolin,J. Doussiere,G. J. M. Lauquin,P. V. Vignaish a large area. In spite of its relatively shallow depth, it is intended as a graduate course. At its present state the amount of material is more thancan be coveredin a one-semestercourse (45h). Two one-quarte978-1-4899-8338-1978-0-387-69931-8

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Analysis of Membrane Antigens by Means of Quantitative Detergent-Immunoelectrophoresishese requirements are difficult to fulfil for most membrane proteins because of the problems involved in their isolation. We have therefore taken an interest in some methods that are not limited by these requirements. In contrast to most other immunological methods, quantitative immunoelectrophoreti

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Separation of Fatty Acids from Plant Membrane Lipids by a Combined GLC-TLC Procedureportant part of the characterization of membrane constituents. Fatty acid mixtures from plant lipids are often quite complex due to the large number of unsaturated components present in these lipids. The scope of the experiment is the separation of fatty acids on the basis of both chain length and u

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Isolation and Purification of the Nicotinic Acetylcholine Receptor from Torpedo Electric Organfied skeletal muscles with a very rich innervation of the cholinergic type. Those from the electric ray . are the richest known source of nAcChR. They contain 12,000–15,000 receptors per μm. on the postsynaptic membrane.

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Preparation of Spectrin-Free Vesicles from Human Red Blood Cellsethods by which such “ghosts” can be prepared have been published by various authors. A summary of some of these methods has been presented by Schwoch and Passow (1973). Intact ghosts, containing all intrinsic (intramembraneous) and extrinsic proteins, as well as cytoskeletal components, can further