Investigating fast enzyme-DNA kinetics using multidimensional fluorescence imaging and microfluidics

2010 ◽  
Author(s):  
Tom Robinson ◽  
Hugh B. Manning ◽  
Christopher Dunsby ◽  
Mark A. A. Neil ◽  
Geoff S. Baldwin ◽  
...  
Keyword(s):  
Fluorescence Imaging ◽  
Multidimensional Fluorescence

scholarly journals Giga-voxel multidimensional fluorescence imaging combining single-pixel detection and data fusion

2021 ◽  
Author(s):  
Fernando Soldevila ◽  
Armin Lenz ◽  
Alberto Ghezzi ◽  
Andrea Farina ◽  
Cosimo D'Andrea ◽  
...  
Keyword(s):  
Data Fusion ◽  
Fluorescence Imaging ◽  
Multidimensional Fluorescence ◽  
Single Pixel

Chapter 4 Multidimensional fluorescence imaging

2009 ◽  
pp. 133-169 ◽  
Author(s):  
James McGinty ◽  
Christopher Dunsby ◽  
Egidijus Auksorius ◽  
Richard K.P. Benninger ◽  
Pieter De Beule ◽  
...  
Keyword(s):  
Fluorescence Imaging ◽  
Multidimensional Fluorescence

Multidimensional Fluorescence Imaging Applied to Biological Tissue

2006 ◽  
pp. 477-524 ◽  
Author(s):  
Daniel S. Elson ◽  
Neil Galletly ◽  
Clifford Talbot ◽  
Jose Requejo-Isidro ◽  
James McGinty ◽  
...  
Keyword(s):  
Fluorescence Imaging ◽  
Biological Tissue ◽  
Multidimensional Fluorescence

scholarly journals Rapid noninvasive monitoring of freshness variation in frozen shrimp using multidimensional fluorescence imaging coupled with chemometrics

Talanta ◽  
2021 ◽  
Vol 224 ◽  
pp. 121871
Author(s):  
Md. Mizanur Rahman ◽  
Minh Vu Bui ◽  
Mario Shibata ◽  
Naho Nakazawa ◽  
Mst. Nazira Akhter Rithu ◽  
...  
Keyword(s):  
Fluorescence Imaging ◽  
Noninvasive Monitoring ◽  
Frozen Shrimp ◽  
Multidimensional Fluorescence

The influence of confocal microscope design on imaging performance

1993 ◽  
Vol 51 ◽  
pp. 144-145
Author(s):  
C J R Sheppard
Keyword(s):  
Image Quality ◽  
Fluorescence Imaging ◽  
Confocal Microscope ◽  
Industrial Applications ◽  
Three Dimensions ◽  
Design Parameters ◽  
Weak Signals ◽  
Size And Shape ◽  
Imaging Performance ◽  
Fundamental Limitation

The confocal microscope is now widely used in both biomedical and industrial applications for imaging, in three dimensions, objects with appreciable depth. There are now a range of different microscopes on the market, which have adopted a variety of different designs. The aim of this paper is to explore the effects on imaging performance of design parameters including the method of scanning, the type of detector, and the size and shape of the confocal aperture.It is becoming apparent that there is no such thing as an ideal confocal microscope: all systems have limitations and the best compromise depends on what the microscope is used for and how it is used. The most important compromise at present is between image quality and speed of scanning, which is particularly apparent when imaging with very weak signals. If great speed is not of importance, then the fundamental limitation for fluorescence imaging is the detection of sufficient numbers of photons before the fluorochrome bleaches.

Ubiquinone-BODIPY nanoparticles for tumor redox-responsive fluorescence imaging and photodynamic activity

2021 ◽  
Author(s):  
Byunghee Hwang ◽  
Tae-Il Kim ◽  
Hyunjin Kim ◽  
Sungjin Jeon ◽  
Yongdoo Choi ◽  
...  
Keyword(s):  
Fluorescence Imaging ◽  
Selective Activation ◽  
Turn On ◽  
Intracellular Environment ◽  
Redox Responsive ◽  
Photodynamic Activity

A ubiquinone-BODIPY photosensitizer self-assembles into nanoparticles (PS-Q-NPs) and undergoes selective activation within the highly reductive intracellular environment of tumors, resulting in “turn-on” fluorescence and photosensitizing activities.

Semiconductor Quantum Dots for Multicolor Fluorescence Imaging and Spectroscopy of Single Cancer Cells

2003 ◽  
Vol 773 ◽  
Author(s):  
Xiaohu Gao ◽  
Shuming Nie ◽  
Wallace H. Coulter
Keyword(s):  
Quantum Dots ◽  
Cancer Cells ◽  
Fluorescence Imaging ◽  
Organic Dyes ◽  
Fluorescent Proteins ◽  
Single Cells ◽  
Quantitative Imaging ◽  
Semiconductor Quantum Dots ◽  
Single Cancer ◽  
Imaging And Spectroscopy

AbstractLuminescent quantum dots (QDs) are emerging as a new class of biological labels with unique properties and applications that are not available from traditional organic dyes and fluorescent proteins. Here we report new developments in using semiconductor quantum dots for quantitative imaging and spectroscopy of single cancer cells. We show that both live and fixed cells can be labeled with multicolor QDs, and that single cells can be analyzed by fluorescence imaging and wavelength-resolved spectroscopy. These results raise new possibilities in cancer imaging, molecular profiling, and disease staging.

Sign in / Sign up

Export Citation Format

Share Document