000 03930nam a2200397 i 4500
999 _c391538
_d391538
001 391538
003 ES-MaUEC
005 20230704150402.0
006 a|||| o|||| 00| 0
007 cr nn 008mamaa
008 210524s2021 xxua o |||| 0|eng d
020 _a9781071614020
024 7 _a10.1007/978-1-0716-1402-0
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aQH224
_b2021 EB
245 0 0 _aConfocal Microscopy :
_bMethods and Protocols
_cedited by Joseph Brzostowski, Haewon Sohn
250 _a1st edition 2021
264 1 _aNew York, NY
_bSpringer International Publising
_c2021
300 _a1 recurso en línea (XI, 363 páginas)
_b88 ilustraciones, 73 ilustraciones a color
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
_v2304
505 0 _aAdvances in Confocal Microscopy and Selected Applications -- Choosing Fluorescent Probes and Labeling Systems -- General Considerations for Acquiring a Three-color Image by Laser Scanning Confocal Microscopy -- Microfabricated devices for confocal microscopy on biological samples -- Zeiss Airyscan: Optimizing Usage for Fast, Gentle, Super-resolution Imaging -- High-resolution multicolor imaging of mitochondria in lymphocytes -- Protein-Retention Expansion Microscopy (ExM): Scalable and Convenient Super-Resolution Microscopy -- Analysis of B Cell Receptor-Mediated Antigen Extraction by B lymphocytes from Plasma Membrane Sheets Using Confocal Microscopy -- Analysis of Intracellular Vesicles in B Lymphocytes: Antigen Traffic in the Spotlight -- Visualizing Key Signaling Components of Macropinocytosis and Phagocytosis Using Confocal Microscopy in the Model Organism Dictyostelium discoideum -- Imaging GPCR-mediated Signal Events Leading to Chemotaxis and Phagocytosis -- High-throughput Imaging of Arrays of Fluorescently Tagged Yeast Mutant Strains -- Visualizing the Dynamics of T Cell-Dendritic Cell Interactions in Intact Lymph Nodes By Multiphoton Confocal Microscopy -- Studying Neuronal Biology Using Spinning Disc Confocal Microscopy -- Method for Acute Intravital Imaging of the Large Intestine in Live Mice -- Fluorescence Lifetime Imaging as a Non-invasive Tool to Study Plasmodium Falciparum Metabolism -- Developing Analysis Protocols for Monitoring Intracellular Oxygenation using Fluorescence Lifetime Imaging of Myoglobin-mCherry -- FLIM Imaging for Metabolic Studies in Live Cells -- A Step by Step Guide to Instant Structured Illumination Microscopy (ISIM).
520 _aThis volume provides a wide range of imaging protocols that can be tailored to specific organisms or cell-types. Chapters guide readers through fixed-cell, live-cell, phenotype screening, super-resolution, intravital imaging techniques, and fluorescence life-time imaging microscopy (FLIM). Written in the highly successful Methods in Molecular Biology series format, chapters include 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, Confocal Microscopy: Methods and Protocols aims to ensure successful results in the further study of this vital field.
988 _aSpringer_Protocols_2021
650 7 _2embne
_9163357
_aMicroscopía confocal
776 0 8 _iPrinted edition:
_z9781071614013
776 0 8 _iPrinted edition:
_z9781071614037
776 0 8 _iPrinted edition:
_z9781071614044
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-1-0716-1402-0
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
998 _b07/2023
_dz
_eb
_zSI