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Cellular Fatty Acid-Binding Proteins II - Proceedings of the 2nd International Workshop on Fatty Acid-Binding Proteins, Maastricht, August 31 and September 1, 1992 (Paperback, Softcover reprint of the original 1st ed. 1993) Loot Price: R5,452
Discovery Miles 54 520
Cellular Fatty Acid-Binding Proteins II - Proceedings of the 2nd International Workshop on Fatty Acid-Binding Proteins,...

Cellular Fatty Acid-Binding Proteins II - Proceedings of the 2nd International Workshop on Fatty Acid-Binding Proteins, Maastricht, August 31 and September 1, 1992 (Paperback, Softcover reprint of the original 1st ed. 1993)

Jan F.C. Glatz, Ger J. Van Der Vusse

Series: Developments in Molecular and Cellular Biochemistry, 10

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Loot Price R5,452 Discovery Miles 54 520 | Repayment Terms: R511 pm x 12*

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The cellular functions of lipid-transport proteins cannot can be obtained, as well as structural information re- garding the local environment of the spectroscopic be fully realized without a comprehensive knowledge of probe. However, changes in protein fluorescence upon their binding properties. In particular, it is important to identify physiologically important ligands and establish ligand binding are sometimes too small to quantitate. their binding affinities, stoichiometries and specificities. This is particularly true for L-FABP, which has no tryp- Since many lipid-binding proteins exhibit no enzymatic tophan residues. Also, some lipids lack intrinsic fluores- cence or paramagnetic properties, including many lipids activity, binding parameters provide an important quan- titative measure for comparing the 'activity' of various of physiological interest. In such cases, lipid analogues wild-type and mutant forms. For this purpose, binding containing structure-perturbing anthroylxoxy or doxyl assays that are quantitative, accurate and robust are de- probes are required. Lipids that do have intrinsic fluor- sirable. escence, such as parinaric acid, are labile and prone to For the intracellular fatty acid- and lipid-binding pro- oxidation. The binding of native ligands can be moni- teins, a variety of biochemical and biophysical binding tored by isotope-directed NMR techniques, provided assays have been used. The biochemical assays include that enrichment with 13C or another suitable isotope is those based on gel-filtration [1-3], equilibrium dialysis feasible. Although such NMR methods are useful for de- [4], Lipidex [5,6] and liposomes [7].

General

Imprint: Springer-Verlag New York
Country of origin: United States
Series: Developments in Molecular and Cellular Biochemistry, 10
Release date: October 2012
First published: 1993
Editors: Jan F.C. Glatz • Ger J. Van Der Vusse
Dimensions: 279 x 210 x 12mm (L x W x T)
Format: Paperback
Pages: 205
Edition: Softcover reprint of the original 1st ed. 1993
ISBN-13: 978-1-4613-6353-8
Categories: Books > Medicine > Clinical & internal medicine > Cardiovascular medicine
Books > Science & Mathematics > Biology, life sciences > Biochemistry > General
Books > Science & Mathematics > Biology, life sciences > Cellular biology > General
LSN: 1-4613-6353-5
Barcode: 9781461363538

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