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Titlebook: Liposome Methods and Protocols; Subhash C. Basu,Manju Basu Book 2002 Humana Press 2002

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21#
發(fā)表于 2025-3-25 04:06:53 | 只看該作者
Use of Liposomes Containing Carbohydrates for Production of Monoclonal Antibodieson a variety of cells and tissues (.) (.). Functional analysis of glycolipids and glycoproteins has been greatly facilitated by the application of monoclonal antibodies. Monoclonal anticarbohydrate antibodies have been also utilized for expression cloning of glycosyltransferases and related genes (.,.).
22#
發(fā)表于 2025-3-25 11:00:54 | 只看該作者
Micelles and Liposomes in Metabolic Enzyme and Glycolipid Glycosyltransferase AssaysThe use of liposomes has long been in practice for various biochemical purposes including liposome-enzyme targeting into different organelles (.–.). Different aspects of liposome uses are discussed in this book. This chapter is a general review on the use of liposomes in the enzyme assay with emphasis on glycolipid:glycosyltransferases.
23#
發(fā)表于 2025-3-25 15:02:37 | 只看該作者
Liposome Methods and Protocols978-1-59259-175-6Series ISSN 1064-3745 Series E-ISSN 1940-6029
24#
發(fā)表于 2025-3-25 15:53:31 | 只看該作者
Subhash C. Basu,Manju BasuIncludes supplementary material:
25#
發(fā)表于 2025-3-25 20:39:23 | 只看該作者
26#
發(fā)表于 2025-3-26 03:26:05 | 只看該作者
Lipids in Viral Fusionion of envelope protein; lipid-envelope protein interactions; and fusion pore formation and pore widening (..) (.,.). The reader is referred to a number of reviews on viral glycoprotein-mediated membrane fusion (.–.).
27#
發(fā)表于 2025-3-26 06:24:10 | 只看該作者
28#
發(fā)表于 2025-3-26 09:40:44 | 只看該作者
29#
發(fā)表于 2025-3-26 14:08:30 | 只看該作者
Liposomes Containing Ligandsly used to represent three members of this LEC-CAM family: L-, E-, and P-selectin. The lectin character of these cell adhesion molecules (CAMs) makes the selectin family unique among all the known CAM families (.–.).
30#
發(fā)表于 2025-3-26 20:18:35 | 只看該作者
Peptide-Induced Fusion of Liposomesmmunological, biochemical, or biophysical technology. However, our understanding of the mechanisms of biological membrane fusion is still rudimentary, and in this context, the use of artificial membranes such as liposomes and model peptide systems is of great value to simulate proteininduced fusion.
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