✦ LIBER ✦

Analysis of protein mobilities and interactions in living cells by multifocal fluorescence fluctuation microscopy

✍ Scribed by Gerrit Heuvelman; Fabian Erdel; Malte Wachsmuth; Karsten Rippe

Publisher: Springer
Year: 2009
Tongue: English
Weight: 748 KB
Volume: 38
Category: Article
ISSN: 1432-1017
DOI: 10.1007/s00249-009-0499-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Investigation of protein–protein interac

Investigation of protein–protein interactions in living cells by chemical crosslinking and mass spectrometry

✍ Andrea Sinz 📂 Article 📅 2010 🏛 Springer 🌐 English ⚖ 275 KB

Confocal fluorescence microscopy study o

Confocal fluorescence microscopy study of interaction between lens MIP26/AQP0 and crystallins in living cells

✍ Bing-Fen Liu; Jack J Liang 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 225 KB

## Abstract MIP26/AQP0 is the major lens fiber membrane protein and has been reported to interact with many other lens components including crystallins, lipid, and cytoskeletal proteins. Regarding crystallins, many previous reports indicate that MIP26/AQP0 interacts with either only α‐crystallin or

Fluorescence microscopy Methods in Cell

Fluorescence microscopy Methods in Cell Biology 29 Fluorescence microscopy of living cells in culture. Part A: Fluorescence analogs, labeling cells and basic microscopy (1989). Edited by Y.-L. Wang & D. L. Taylor. Academic Press, New York. Pp 333. $59.00

✍ David M. Schotten 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 269 KB 👁 1 views

Fluorescence microscopy revisited Fluore

Fluorescence microscopy revisited Fluorescence Microscopy of Living Cells in Culture, Part B, Quantitative Fluorescence Microscopy – Imaging and spectroscopy (1989). Edited by D. Lansing Taylor and YU-LI Wang. Methods in Cell Biology 30. Academic Press: New York. 503pp. £94

✍ David M. Shotton 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 422 KB 👁 1 views

The fact that ncarly all humans have their heart on the left hand side is taken for granted by most people, without appreciating the complexity of the explanations needed to account for why this is consistently so. In many organisms we can understand, in principle, how the antero-posterior, and dorw

Spontaneous and MNNG-induced reversion o

Spontaneous and MNNG-induced reversion of an EGFP construct in HeLa cells: An assay for observing mutations in living cells by fluorescent microscopy

✍ Federica Gemignani; Stefano Landi; David M. DeMarini; Ryszard Kole 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 457 KB

HeLa cell line stably expressing the enhanced green fluorescence protein (EGFP) gene, interrupted by the HBB IVS2-654 intron, was studied without treatment and after treatment with a single standard dose of 15 mM of N-methyl-N¢-nitro-N-nitrosoguanidine (MNNG). This assay was done in order to prove t

Expression and Analysis of Green Fluores

Expression and Analysis of Green Fluorescent Proteins in Human Embryonic Kidney Cells by Capillary Electrophoresis

✍ Amir Malek; Morteza G. Khaledi 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 115 KB

The green fluorescent protein (GFP) has attracted much interest as a reporter for gene expression. In this paper, application of capillary electrophoresis with laser-induced fluorescent (CE-LIF) for quantitation of green fluorescence protein in cellular extracts and single cells is investigated. The