What it means to measure a single molecule in a solution by fluorescence fluctuation spectroscopy

Experimental and Molecular Pathology

Volumn 80, Issue 3, 2006, Pages 209-218

  Földes Papp, Zeno ^a  

^a MEDICAL UNIVERSITY OF GRAZ   (Austria)

Author keywords

Cellular network; Cutting edge technologies; Fluorescence correlation spectroscopy (FCS); Fluorescence fluctuation spectroscopy; Individual molecule; Meaningful time; Microfluidics; Nanofluidics; Neurodegenerative disease; Neuron; Neurotrophin network; Selfsame molecule likelihood estimators; Selfsame single molecule regime; Single (solution) phase single molecule fluorescence auto and two color cross correlation spectroscopy (SPSM FCS); Single molecule analysis; Two color fluorescence cross correlation spectroscopy (FCCS)

Indexed keywords

NEUROTROPHIN; QUANTUM DOT;

BIOTECHNOLOGY; CELL HETEROGENEITY; CHEMICAL STRUCTURE; CYTOLOGY; DEGENERATIVE DISEASE; FLUORESCENCE CORRELATION SPECTROSCOPY; FLUORESCENCE SPECTROSCOPY; GENE AMPLIFICATION; GENE TECHNOLOGY; HYDRODYNAMICS; HYPOTHESIS; LABORATORY; MICROFLUIDIC ANALYSIS; MOLECULAR BIOLOGY; MOLECULAR CLONING; MOLECULAR DYNAMICS; MOLECULAR PROBE; MOLECULE; PARAMETER; POLYMERASE CHAIN REACTION; REVIEW; THEORETICAL STUDY;

FLUORESCENT DYES; MODELS, CHEMICAL; NANOTECHNOLOGY; SPECTROMETRY, FLUORESCENCE;

EID: 33646495986     PISSN: 00144800     EISSN: 10960945     Source Type: Journal    
DOI: 10.1016/j.yexmp.2006.01.001     Document Type: Review

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