Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Mark A. Naivar"'
Autor:
Kimberly L. Foster, Mark A. Naivar, Kevin Shields, Jennifer L. Walker, Luke H. C. Patterson, Evelyn Rodriguez-Mesa, Adele M. Doyle, Mehran R. Hoonejani, Megan T. Valentine, John S. Foster
Publikováno v:
Biomedical Microdevices. 22
Although microfluidic micro-electromechanical systems (MEMS) are well suited to investigate the effects of mechanical force on large populations of cells, their high-throughput capabilities cannot be fully leveraged without optimizing the experimenta
Publikováno v:
Cytometry
Fluorescence lifetime measurements provide information about the fluorescence relaxation, or intensity decay, of organic fluorophores, fluorescent proteins, and other inorganic molecules that fluoresce. The fluorescence lifetime is emerging in flow c
Publikováno v:
Cytometry Part A. :253-264
There is a long standing interest in measuring complete emission spectra from individual cells in flow cytometry. We have developed flow cytometry instruments and analysis approaches to enable this to be done routinely and robustly. Our spectral flow
Autor:
Travis A. Woods, Steven W. Graves, Robert C. Habbersett, John P. Nolan, Mark A. Naivar, David S. Sebba, Mark E. Wilder
Publikováno v:
Cytometry Part A. :979-989
Fully digital data acquisition systems for use in flow cytometry provide excellent flexibility and precision. Here, we demonstrate the development of a low cost, small, and low power digital flow cytometry data acquisition system using a single micro
Autor:
Larry A. Sklar, Bruce S. Edwards, Mark A. Naivar, John C. Martin, Robert C. Habbersett, James H. Jett, Jimmie D. Parson, James P. Freyer, Mark E. Wilder, Steven W. Graves, John P. Nolan
Publikováno v:
Cytometry Part A. :915-924
A digital signal processing (DSP)-based digital data acquisition system has been developed to support novel flow cytometry efforts. The system flexibility includes how it detects, captures, and processes event data. Custom data capture boards utilizi
Illustration of a flow cytometer capable of capturing multiple fluorescence lifetime measurements; creating potential for multi-parametric, time-resolved signals to be captured for every color channel. Flow cytometry is a powerful means for in vitro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c67220cf6ea04da7cb1e17a9a21118df
https://europepmc.org/articles/PMC4869968/
https://europepmc.org/articles/PMC4869968/
Autor:
Mark A. Naivar, David W. Galbraith
Publikováno v:
Current Protocols in Cytometry
A flow cytometer is made up of many different subsystems that work together to measure the optical properties of individual cells within a sample. The data acquisition system (also called the data system) is one of these subsystems, and it is respons
Autor:
James H. Jett, Robb Habbersett, Mark A. Naivar, Steven W. Graves, Peter M. Goodwin, John P. Nolan, John C. Martin, Gregory Goddard
Publikováno v:
Cytometry Part A. :842-851
Background: While conventional multiparameter flow cytometers have proven highly successful, there are several types of analytical measurements that would benefit from a more comprehensive and flexible approach to spectral analysis including, but cer
Autor:
William J. Peria, Ruofan Cao, Jessica P. Houston, Patrick Jenkins, Bryan Sands, Roger Brent, Mark A. Naivar
Publikováno v:
Optics Express. 24:14596
Interest in time resolved flow cytometry is growing. In this paper, we collect time-resolved flow cytometry data and use it to create polar plots showing distributions that are a function of measured fluorescence decay rates from individual fluoresce
Publikováno v:
Current Protocols in Cytometry
In flow cytometry, the fluorescence decay time of an excitable species has been largely underutilized and is not likely found as a standard parameter on any imaging cytometer, sorting, or analyzing system. Most cytometers lack fluorescence lifetime h