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pro vyhledávání: '"Anthony Tsikouras"'
Publikováno v:
Photonics, Vol 3, Iss 4, p 56 (2016)
Current instruments used to detect specific protein-protein interactions in live cells for applications in high-content screening (HCS) are limited by the time required to measure the lifetime. Here, a 32 × 1 single-photon avalanche diode (SPAD) arr
Externí odkaz:
https://doaj.org/article/0c97f707bf524ea4b9d9cfe8b78f2a37
Autor:
Nehad Hirmiz, Elizabeth J Osterlund, Morgan Richards, David W. Andrews, Qiyin Fang, Anthony Tsikouras
Publikováno v:
IEEE Journal of Selected Topics in Quantum Electronics. 27:1-9
Protein-protein interactions can be measured in live cells, at nanometer scale, using Fluorescence Lifetime Imaging Microscopy (FLIM) enabled Forster Resonance Energy Transfer (FRET). There are growing interests in exploring protein-protein interacti
Autor:
Anthony Tsikouras, Qiyin Fang, Nehad Hirmiz, David W. Andrews, Elizabeth J Osterlund, Morgan Richards
Publikováno v:
Optics express. 27(16)
The streak camera is a picosecond resolution photodetector with parallel input capability; however, the degree of multiplexing is limited by crosstalk and temporal uncertainty in the sweeping field. We introduced a fixed time delay between adjacent f
Autor:
Elizabeth J Osterlund, Nehad Hirmiz, Qiyin Fang, Anthony Tsikouras, Jessica Kun, Morgan Richards, David W. Andrews
Publikováno v:
Advances in Microscopic Imaging II.
Quantitative measurement of protein-protein interaction is important for many biological processes, including cell growth, intercellular communication, gene expression and apoptosis. Forster Resonance Energy Transfer (FRET) provides a molecular level
Autor:
Qiyin Fang, Anthony Tsikouras, David W. Andrews, Elizabeth J Osterlund, Nehad Hirmiz, Morgan Richards
Publikováno v:
Optics Letters. 45:69
Currently, the spinning disk confocal microscope is the most popular fast confocal imaging system. However, these instruments require a high pixel density camera detector, limiting their use in many applications. We have designed a multiplexed confoc
Publikováno v:
Photonics; Volume 3; Issue 4; Pages: 56
Photonics, Vol 3, Iss 4, p 56 (2016)
Photonics, Vol 3, Iss 4, p 56 (2016)
Current instruments used to detect specific protein-protein interactions in live cells for applications in high-content screening (HCS) are limited by the time required to measure the lifetime. Here, a 32 × 1 single-photon avalanche diode (SPAD) arr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc3389b6bd7981b60e8bda016540de5
http://hdl.handle.net/11311/1009652
http://hdl.handle.net/11311/1009652
Publikováno v:
Biomedical optics express. 6(10)
Confocal microscopy has several advantages over wide-field microscopy, such as out-of-focus light suppression, 3D sectioning, and compatibility with specialized detectors. While wide-field microscopy is a faster approach, multiplexed confocal schemes
Publikováno v:
ECS Meeting Abstracts. :1487-1487
Fluorescence lifetime imaging microscopy (FLIM) is a powerful imaging modality that can provide unique information related to the biological microenvironment of a sample. For instance, when applied to quantifying Förster resonant energy transfer (FR
Publikováno v:
ResearcherID
The streak camera is one of the fastest photodetection systems, while its capability of multiplexing is particularly attractive to many applications requiring parallel data acquisition. The degree of multiplexing in a streak camera is limited by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d3387c9e30e60b6a3f31d680d11be1a
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000299818600044&KeyUID=WOS:000299818600044
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000299818600044&KeyUID=WOS:000299818600044