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Two-photon fluorescent labels with enhanced sensitivity for biological imaging
The development of two-photon laser scanning fluorescence microscopy (TPLSM) has provided a new capability for 3D imaging in whole and living tissues, reduced photobleaching effects, and greater depth penetration. Since the rate of two-photon excitation is proportional to the square of the light int...
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container_end_page | 331 vol.1 |
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creator | Wenseleers, W. Stellacci, F. Pond, S. Parker, T. Mangel, T. Halik, M. Meyer-Friedrichsen, T. Perry, J.W. Marder, S.R. Heikal, A.A. Shaohui Huang Webb, W.W. |
description | The development of two-photon laser scanning fluorescence microscopy (TPLSM) has provided a new capability for 3D imaging in whole and living tissues, reduced photobleaching effects, and greater depth penetration. Since the rate of two-photon excitation is proportional to the square of the light intensity, degree of excitation falls off roughly as the fourth power of distance from the focal plane. The full potential of two-photon fluorescence microscopy has not been realized, in part, because fluorophores under use have been developed for single photon excitation and have not been optimized for two-photon absorption. Highly efficient two-photon fluorophores are needed to allow sensitive detection of small numbers of labeled sites and to reduce the optical power of the exciting laser beam that is needed to produce adequate signal levels. The sensitivity of a two-photon fluorescence label is determined by the product of the two-photon absorption cross section and the fluorescence quantum efficiency. |
doi_str_mv | 10.1109/LEOS.2000.890812 |
format | conference_proceeding |
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Since the rate of two-photon excitation is proportional to the square of the light intensity, degree of excitation falls off roughly as the fourth power of distance from the focal plane. The full potential of two-photon fluorescence microscopy has not been realized, in part, because fluorophores under use have been developed for single photon excitation and have not been optimized for two-photon absorption. Highly efficient two-photon fluorophores are needed to allow sensitive detection of small numbers of labeled sites and to reduce the optical power of the exciting laser beam that is needed to produce adequate signal levels. The sensitivity of a two-photon fluorescence label is determined by the product of the two-photon absorption cross section and the fluorescence quantum efficiency.</description><subject>Absorption</subject><subject>Biological systems</subject><subject>Biomedical optical imaging</subject><subject>Charge transfer</subject><subject>Diagnosis</subject><subject>Diseases</subject><subject>Fluorescence</subject><subject>Laser beams</subject><subject>Laser excitation</subject><subject>Microscopic examination</subject><subject>Microscopy</subject><subject>Optical imaging</subject><subject>Optical sensors</subject><subject>Quantum efficiency</subject><subject>Solvents</subject><issn>1092-8081</issn><issn>2766-1733</issn><isbn>9780780359475</isbn><isbn>078035947X</isbn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2000</creationdate><recordtype>conference_proceeding</recordtype><sourceid>6IE</sourceid><recordid>eNotkD1rwzAQhkU_oGmavXTS1M3uSbItaSwh_YDQDE1nI9vnREWxUktpyL-vIIV7ueW5l4cj5J5Bzhjop-Vi9ZlzAMiVBsX4BZlwWVUZk0JckpmWCtKIUheyvCKTdMIzlcAbchvCNwAHLuWEfKyPPttvffQD7d3BjxhaHCJ1pkEX6NHGLcVha4YWOxpwCDbaXxtPtPcjbax3fmNb46jdmY0dNnfkujcu4Ox_T8nXy2I9f8uWq9f3-fMysxxEzPoGBcq-1EylFEIpjUnWNB1DANmaUhZ9pTuEroSq6XpodWck06xVVcsbMSWP59796H8OGGK9s0ncOTOgP4Sas6KEopAJfDiDFhHr_Zg8x1N9fpn4A01OXpM</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>Wenseleers, W.</creator><creator>Stellacci, F.</creator><creator>Pond, S.</creator><creator>Parker, T.</creator><creator>Mangel, T.</creator><creator>Halik, M.</creator><creator>Meyer-Friedrichsen, T.</creator><creator>Perry, J.W.</creator><creator>Marder, S.R.</creator><creator>Heikal, A.A.</creator><creator>Shaohui Huang</creator><creator>Webb, W.W.</creator><general>IEEE</general><scope>6IE</scope><scope>6IH</scope><scope>CBEJK</scope><scope>RIE</scope><scope>RIO</scope></search><sort><creationdate>2000</creationdate><title>Two-photon fluorescent labels with enhanced sensitivity for biological imaging</title><author>Wenseleers, W. ; Stellacci, F. ; Pond, S. ; Parker, T. ; Mangel, T. ; Halik, M. ; Meyer-Friedrichsen, T. ; Perry, J.W. ; Marder, S.R. ; Heikal, A.A. ; Shaohui Huang ; Webb, W.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i203t-fbe3e7f591859143889e803abd1e007ca574f69de0d506bdf0c9da7191c86c2b3</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Absorption</topic><topic>Biological systems</topic><topic>Biomedical optical imaging</topic><topic>Charge transfer</topic><topic>Diagnosis</topic><topic>Diseases</topic><topic>Fluorescence</topic><topic>Laser beams</topic><topic>Laser excitation</topic><topic>Microscopic examination</topic><topic>Microscopy</topic><topic>Optical imaging</topic><topic>Optical sensors</topic><topic>Quantum efficiency</topic><topic>Solvents</topic><toplevel>online_resources</toplevel><creatorcontrib>Wenseleers, W.</creatorcontrib><creatorcontrib>Stellacci, F.</creatorcontrib><creatorcontrib>Pond, S.</creatorcontrib><creatorcontrib>Parker, T.</creatorcontrib><creatorcontrib>Mangel, T.</creatorcontrib><creatorcontrib>Halik, M.</creatorcontrib><creatorcontrib>Meyer-Friedrichsen, T.</creatorcontrib><creatorcontrib>Perry, J.W.</creatorcontrib><creatorcontrib>Marder, S.R.</creatorcontrib><creatorcontrib>Heikal, A.A.</creatorcontrib><creatorcontrib>Shaohui Huang</creatorcontrib><creatorcontrib>Webb, W.W.</creatorcontrib><collection>IEEE Electronic Library (IEL) Conference Proceedings</collection><collection>IEEE Proceedings Order Plan (POP) 1998-present by volume</collection><collection>IEEE Xplore All Conference Proceedings</collection><collection>IEEE Xplore</collection><collection>IEEE Proceedings Order Plans (POP) 1998-present</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Wenseleers, W.</au><au>Stellacci, F.</au><au>Pond, S.</au><au>Parker, T.</au><au>Mangel, T.</au><au>Halik, M.</au><au>Meyer-Friedrichsen, T.</au><au>Perry, J.W.</au><au>Marder, S.R.</au><au>Heikal, A.A.</au><au>Shaohui Huang</au><au>Webb, W.W.</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>Two-photon fluorescent labels with enhanced sensitivity for biological imaging</atitle><btitle>CONF PROC LASER ELECTR OPTIC SOC ANNU MEET CLEO</btitle><stitle>LEOS</stitle><date>2000</date><risdate>2000</risdate><volume>1</volume><spage>330</spage><epage>331 vol.1</epage><pages>330-331 vol.1</pages><issn>1092-8081</issn><eissn>2766-1733</eissn><isbn>9780780359475</isbn><isbn>078035947X</isbn><notes>SourceType-Books-1</notes><notes>ObjectType-Book-1</notes><notes>content type line 25</notes><notes>ObjectType-Conference-2</notes><notes>SourceType-Conference Papers & Proceedings-2</notes><abstract>The development of two-photon laser scanning fluorescence microscopy (TPLSM) has provided a new capability for 3D imaging in whole and living tissues, reduced photobleaching effects, and greater depth penetration. Since the rate of two-photon excitation is proportional to the square of the light intensity, degree of excitation falls off roughly as the fourth power of distance from the focal plane. The full potential of two-photon fluorescence microscopy has not been realized, in part, because fluorophores under use have been developed for single photon excitation and have not been optimized for two-photon absorption. Highly efficient two-photon fluorophores are needed to allow sensitive detection of small numbers of labeled sites and to reduce the optical power of the exciting laser beam that is needed to produce adequate signal levels. The sensitivity of a two-photon fluorescence label is determined by the product of the two-photon absorption cross section and the fluorescence quantum efficiency.</abstract><pub>IEEE</pub><doi>10.1109/LEOS.2000.890812</doi><tpages>2</tpages></addata></record> |
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source | IEEE Electronic Library (IEL) Conference Proceedings |
subjects | Absorption Biological systems Biomedical optical imaging Charge transfer Diagnosis Diseases Fluorescence Laser beams Laser excitation Microscopic examination Microscopy Optical imaging Optical sensors Quantum efficiency Solvents |
title | Two-photon fluorescent labels with enhanced sensitivity for biological imaging |
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