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Measuring biological responses with automated microscopy /
The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now wit...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
San Diego, California :
Elsevier/Academic Press,
[2006]
|
| Colección: | Methods in enzymology ;
v. 414. |
| Temas: | |
| Acceso en línea: | Texto completo Texto completo Texto completo |
MARC
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| 245 | 0 | 0 | |a Measuring biological responses with automated microscopy / |c edited by James Inglese. |
| 264 | 1 | |a San Diego, California : |b Elsevier/Academic Press, |c [2006] | |
| 264 | 4 | |c �2006 | |
| 300 | |a 1 online resource (xliv, 691 pages) : |b illustrations (some color) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 347 | |a text file | ||
| 490 | 1 | |a Methods in enzymology, |x 0076-6879 ; |v v. 414 | |
| 504 | |a Includes bibliographical references and indexes. | ||
| 505 | 0 | |a Dynamic green fluorescent protein sensors for high-content analysis of the cell cycle / S. Stubbs [and others] -- High-content fluorescence-based screening for epigenetic modulators / E.D. Martinez [and others] -- Development of assays for nuclear receptor modulators using fluorescently tagged proteins / E.D. Martinez [and others] -- The ligand-independent translocation assay: An enabling technology for screening orphan g protein-coupled receptors by arrestin recruitment / R.H. Oakley [and others] -- High-content screening of known g protein-coupled receptors by arrestin translocation / C.C. Hudson [and others] -- Cell imaging assays for g protein-coupled receptor internalization: Application to high-throughput screening / S. Lee [and others] -- High-throughput confocal microscopy for b arrestin-green fluorescent protein translocation g protein-coupled receptor assays using the evotec opera / R.J. Garippa [and others] -- G protein-coupled receptor internalization assays in the high-content screening format / D. Haasen [and others] -- Screening for activators of the wingless type/frizzled pathway by automated fluorescent microscopy / K.M. Borchert [and others] -- A live cell, image-based approach to understanding the enzymology and pharmacology of 2-bromopalmitate and palmitoylation / I. Mikic [and others] -- High-resolution-throughput microscopy analyses of nuclear receptor and coregulator function / V. Berno [and others] -- Tracking individual proteins in living cells using single quantum dot imaging / S. Courty [and others] -- Development and application of automatic high-resolution light microscopy for cell-based screens / Y. Paran [and others] -- Adenoviral sensors for high[hyphen (true graphic)]content cellular analysis / J.M. Kendall [and others] -- Cell-based assays using primary endothelial cells to study multiple steps in inflammation / T. Mayer [and others] -- Development and implementation of multiplexed cell-based imaging assays / B.J. Howell [and others] -- High-throughput screening for modulators of stem cell differentiation / P.J. Bushway [and others] -- High-content kinetic calcium imaging in drug-sensitive and drug-resistant human breast cancer cells / M.A. DeBernardi [and others] -- Measurement and analysis of calcium signaling in heterogeneous cell cultures / G.R. Richards [and others] -- Multiplex analysis of inflammatory signaling pathways using a high-content imaging system / M. Bertelsen [and others] -- Generation and characterization of a stable mk2-egfp cell line and subsequent development of a high-content imaging assay on the cellomics arrayscan platform to screen for p38 mitogen-activated protein kinase inhibitors / R.G. Williams [and others] -- Development and implementation of three mitogen[hyphen-activated protein kinase (mapk) signaling pathway imaging assays to provide mapk module selectivity profiling for kinase inhibitors: Mk2-egfp translocation, c-jun, and erk activation / D. Nickischer [and others] -- Assay development and case history of a 32k-biased library high-content mk2-egfp translocation screen to identify p38 mitogenactivated protein kinase inhibitors on the arrayscan 3.1 imaging platform / J.O.J. Trask [and others] -- Compound classification using image-based cellular phenotypes / C.L. Adams [and others] -- High-content screening: Emerging hardware and software technologies / S. Lee [and others] -- An infrastructure for high-throughput microscopy: Instrumentation, informatics, and integration / E.A. Vaisberg [and others] -- Protein translocation assays: Key tools for accessing new biological information with high-throughput microscopy / A. Heydorn [and others] -- High-content screening of functional genomic libraries / D.R. Rines [and others] -- Fluorescent protein-based cellular assays analyzed by laser-scanning microplate cytometry in 1536-well plate format / D.S. Auld [and others] -- High-throughput measurements of biochemical responses using the plate::Vision multimode 96 minilens array reader / K. Huang [and others] -- Systems cell biology based on high-content screening / K.A. Giuliano [and others] -- Digital autofocus methods for automated microscopy / F. Shen [and others] -- Fluorescence lifetime imaging microscopy: Two-dimensional distribution measurement of fluorescence lifetime / M. Fujiwara [and others]. | |
| 588 | 0 | |a Print version record. | |
| 520 | |a The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with more than 300 volumes (all of them still in print), the series contains much material still relevant today-truly an essential publication for researchers in all fields of life sciences. | ||
| 546 | |a English. | ||
| 650 | 0 | |a Microscopy |x Technique. | |
| 650 | 0 | |a Enzymology |x Equipment and supplies. | |
| 650 | 0 | |a Cell physiology. | |
| 650 | 0 | |a Automation. | |
| 650 | 0 | |a Cells. | |
| 650 | 1 | 2 | |a Cell Physiological Phenomena |0 (DNLM)D002468 |
| 650 | 1 | 2 | |a Microscopy, Fluorescence |x methods |0 (DNLM)D008856Q000379 |
| 650 | 2 | 2 | |a Automation |0 (DNLM)D001331 |
| 650 | 2 | 2 | |a Cells |0 (DNLM)D002477 |
| 650 | 2 | 2 | |a Microscopy, Fluorescence |x instrumentation |0 (DNLM)D008856Q000295 |
| 650 | 6 | |a Microscopie |x Technique. |0 (CaQQLa)201-0038469 | |
| 650 | 6 | |a Cellules |x Physiologie. |0 (CaQQLa)201-0005055 | |
| 650 | 6 | |a Automatisation. |0 (CaQQLa)201-0002748 | |
| 650 | 6 | |a Cellules. |0 (CaQQLa)201-0005079 | |
| 650 | 7 | |a automation. |2 aat |0 (CStmoGRI)aat300056084 | |
| 650 | 7 | |a SCIENCE |x Microscopes & Microscopy. |2 bisacsh | |
| 650 | 7 | |a Cells. |2 fast |0 (OCoLC)fst00850250 | |
| 650 | 7 | |a Cell physiology. |2 fast |0 (OCoLC)fst00850214 | |
| 650 | 7 | |a Automation. |2 fast |0 (OCoLC)fst00822786 | |
| 650 | 7 | |a Microscopy |x Technique. |2 fast |0 (OCoLC)fst01020073 | |
| 700 | 1 | |a Inglese, James, |e editor. | |
| 776 | 0 | 8 | |i Print version: |t Measuring biological responses with automated microscopy. |d San Diego, California : Elsevier/Academic Press, �2006 |z 0121828190 |w (OCoLC)74428888 |
| 830 | 0 | |a Methods in enzymology ; |v v. 414. |x 0076-6879 | |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780121828196 |z Texto completo |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/bookseries/00766879/414 |z Texto completo |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/bookseries/00766879 |z Texto completo |