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Titlebook: Caspases,Paracaspases, and Metacaspases; Methods and Protocol Peter V. Bozhkov,Guy Salvesen Book 2014 Springer Science+Business Media New Y

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发表于 2025-3-21 18:56:09 | 显示全部楼层 |阅读模式
书目名称Caspases,Paracaspases, and Metacaspases
副标题Methods and Protocol
编辑Peter V. Bozhkov,Guy Salvesen
视频video
概述Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the expert.Includes supplementary material
丛书名称Methods in Molecular Biology
图书封面Titlebook: Caspases,Paracaspases, and Metacaspases; Methods and Protocol Peter V. Bozhkov,Guy Salvesen Book 2014 Springer Science+Business Media New Y
描述.Caspases, Paracaspases, and Metacaspacses: Methods and Protocols. is a collection of laboratory protocols covering current methods that are employed to measure and detect activities of these proteases in diverse biological systems, ranging from unicellular organisms to mammals. Broken into two parts, the first part focuses on methods to measure, detect, and inhibit activation and activity of a subset of or specific caspases .in vitro. and in several model systems and organisms, primarily in the context of programmed cell death. The second part of the book provides experimental protocols for purification and .in vitro. and .in vivo. analysis of yeast, protozoan and plant metacaspases, as well as of a human paracaspase MALT1. Written in the highly successful .Methods in Molecular Biology. series format, the chapters include the kind of detailed description and implementation advice that is crucial for getting optimal results in the laboratory..Authoritative and practical, .Caspases, Paracaspases, and Metacaspacses: Methods and Protocols. seeks to aid scientists easy-to-follow techniques..
出版日期Book 2014
关键词caspase substrate; caspases; human paracaspase MALT1; in vitro and in vivo analysis of yeast; metacaspas
版次1
doihttps://doi.org/10.1007/978-1-4939-0357-3
isbn_softcover978-1-4939-5405-6
isbn_ebook978-1-4939-0357-3Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2014
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Positional Scanning Substrate Combinatorial Library (PS-SCL) Approach to Define Caspase Substrate Spscribe the protocol for analyzing S4-S2 pockets preferences of caspases using PS-SCL. Additionally, we describe procedures for the identification of optimal substrates sequence after PS-SCL, solid phase synthesis, and purification of selected fluorogenic substrates, as well as their kinetic analysis
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Methods for the Study of Caspase Activation in the , Oocyte and Egg Extractificantly contributed to these advances. Twenty years ago, Newmeyer and colleagues first showed that the . egg extract, when incubated at room temperature, reconstituted the key molecular events of cellular apoptosis including cytochrome . release, nuclear condensation, internucleosomal fragmentatio
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Caspase Protocols in Mice apoptotic pathway. Since the discovery of caspases, many methods have been developed to detect their activation and are widely used in basic and clinical studies. In a mouse tissue, caspase activation can be monitored by cleavage of caspase-specific synthetic substrates and by detecting cleaved cas
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Measurement of Caspase Activation in Mammalian Cell Culturesleaving protein substrates harboring specific target motifs. Basically all biochemical and morphological changes in an apoptotic cell, including cell shrinkage, chromatin condensation, DNA fragmentation, and plasma membrane blebbing, are consequence of caspase-mediated proteolysis. Thus, uncovering
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Detection and Measurement of Paracaspase MALT1 Activity the immune response. Oncogenic activation of MALT1 is associated with the development of specific forms of B-cell lymphomas. Through specific cleavage of its substrates, MALT1 controls various aspects of lymphocyte activation, including the activation of transcriptional pathways, the stabilization
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Metacaspase: An Arginine-Specific Peptidaseole of metacaspase in . is still a matter of debate, whereas its peptidase enzymatic activity has been well characterized. Among the different possible expression systems, metacaspase-deficient yeast cells (.) have been instrumental in studying the activity of . metacaspase (LmjMCA). Here, we descri
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