000			04085nam a22003735i 4500
001			234052
003			ES-VaUE
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007			cr nn 008mamaa
008			110907s2011 xxu| s |||| 0|eng d
020			_a9781617792953
024	7		_a10.1007/978-1-61779-295-3 _2doi
040			_aES-MaUEC _bspa _cES-MaUEC
245	1	0	_aMolecular Chaperones _bMethods and Protocols _cedited by Stuart K. Calderwood, Thomas L. Prince.
250			_a1st edition 2011
264		1	_aTotowa, NJ _bHumana Press _c2011
300			_a1 recurso en línea (XVIII, 320 páginas) _b42 ilustraciones
336			_atexto _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
347			_aarchivo de texto _bPDF
490	0		_aMethods in Molecular Biology _x1940-6029 _v787
505	0		_aTargeted Deletion of Hsf1, 2, and 4 Genes in Mice -- The Role Of Heat Shock Factors in Stress-Induced Transcription -- Hsp90 and Client Protein Maturation.- The Role of p23, Hop, Immunophilins, and Other Co-Chaperones in Regulating Hsp90 Function -- Detecting Hsp90 Phosphorylation -- Role of Molecular Chaperones in Biogenesis of the Protein Kinome -- Nucleotide Exchange Factors for Hsp70 Chaperones -- Reconstitution of CHIP E3 Ubiquitin Ligase Activity -- Structure-Functions of HspB1 (Hsp27) -- Combined Lentiviral and RNAi Technologies for the Delivery and Permanently Silencing of the hsp25 Gene -- Quantification of HSP27 and HSP70 Molecular Chaperone Activities -- Measuring Hsp72 (HSPA1A) by Indirect Sandwich ELISA -- Analysis of Heat Shock Protein Localization Using Flow Cytometry -- Quantitation of Heat Shock Proteins in Clinical Samples Using Mass Spectrometry -- Bioinformatic Approach to Identify Chaperone Pathway Relationship from Large-Scale Interaction Networks -- Hsp70: Anti-Apoptotic and Tumorigenic Protein -- Determination of Cell Survival or Death -- Immunohistochemistry of Human Hsp60 in Health and Disease: From Autoimmunity to Cancer -- Preparation of a Heat Shock Proteins 70-Based Vaccine from DC-Tumor Fusion Cells -- Isolation of Heat Shock Protein Complexes -- Enhancing Antigen Cross-Presentation and T-Cell Priming by Complexing Protein Antigen to Recombinant Large Heat Shock Protein -- Investigating Receptors for Extracellular Heat Shock Proteins -- Analysis of Cellular Migration Using a Two-Chamber Methodology.
520			_aThe proteome consists of a complex mixture of proteins each of which need to be folded correctly in order to function for the health of the organism, and many of these proteins require molecular chaperones to reach the correct conformation and, in some cases, to remain in a folded form.  In Molecular Chaperones: Methods and Protocols, expert researchers address a wide variety of approaches to the study these mechanisms, featuring the workings of heat shock proteins and heat shock transcription factors, in vitro and in vivo. Written in the highly successful Methods in Molecular Biology™ series format, chapters features introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.   Authoritative and cutting-edge, Molecular Chaperones: Methods and Protocols serves as an ideal guide for all scientists who wish to pursue this vital biological action and its impact on human health and disease.
700	1		_aCalderwood, Stuart K _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt
700	1		_aPrince, Thomas L _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt
776	0	8	_iPrinted edition: _z9781617792946
776	0	8	_iPrinted edition: _z9781617792960
776	0	8	_iPrinted edition: _z9781493961702
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-1-61779-295-3 _z(usuarios Universidad Europea de Valencia)
942			_2lcc _cLE
988			_aSpringer_Protocols_2011
999			_c234052 _d234052