Fluorescence microscope light source stability
The process of fluorescence starts with the efficient generation of light that is required for the excitation of fluorophores. As such, light sources are a crucial component of a fluorescence microscope. Choosing the right illumination tool can not only improve the quality of experimental results, b...
Gespeichert in:
Veröffentlicht in: | Histochemistry and cell biology 2019-04, Vol.151 (4), p.357-366 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 366 |
---|---|
container_issue | 4 |
container_start_page | 357 |
container_title | Histochemistry and cell biology |
container_volume | 151 |
creator | Mubaid, Firas Kaufman, Daniel Wee, Tse-Luen Nguyen-Huu, Dong-Son Young, David Anghelopoulou, Maria Brown, Claire M. |
description | The process of fluorescence starts with the efficient generation of light that is required for the excitation of fluorophores. As such, light sources are a crucial component of a fluorescence microscope. Choosing the right illumination tool can not only improve the quality of experimental results, but also the microscope’s economic and environmental footprint. While arc lamps have historically proven to be a reliable light source for widefield fluorescence microscopy, solid-state light-emitting diodes (LEDs) have become the light source of choice for new fluorescence microscopy systems. In this paper, we demonstrate that LEDs have superior light stability on all timescales tested and use less electrical power than traditional light sources when used at lower power outputs. They can be readily switched on and off electronically, have a longer lifetime and they do not contain mercury, and thus are better for the environment. We demonstrate that it is important to measure light source power output during warm-up and switching, as a light source’s responsiveness (in terms of power) can be quite variable. Several general protocols for testing light source stability are presented. A detailed life cycle analysis shows that an LED light source can have a fourfold lower environmental impact when compared to a metal halide source. |
doi_str_mv | 10.1007/s00418-019-01776-6 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2210008861</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2180265128</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-62e0b2dad43176738d623f65614287b33c2ffcbde0a4768180abe9d7617aec763</originalsourceid><addsrcrecordid>eNp9kE9LwzAYh4Mobk6_gAcZePHS-SZpk_Qow6kw8KLgLaRpOjv6ZybtYd_et3YqePAQAsmT3_vLQ8glhQUFkLcBIKYqApriklJE4ohMacxZRGn6dkymkMYqEngyIWchbAFokjJ2SiYcpJCQwJQsVlXfehesa6yb16X1bbDtzs2rcvPezUPbezwPncnKquz25-SkMFVwF4d9Rl5X9y_Lx2j9_PC0vFtHlsukiwRzkLHc5DGnOImrXDBeiAS7MCUzzi0rCpvlDkwshaIKTObSXAoqjbNS8Bm5GXN3vv3oXeh0XWLHqjKNa_ugGUMDoJSgiF7_QbdYusF2mmEwEwllCik2UsMHg3eF3vmyNn6vKejBph5tarSpv2zqocXVIbrPapf_PPnWhwAfgYBXzcb539n_xH4Crf9-AQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2180265128</pqid></control><display><type>article</type><title>Fluorescence microscope light source stability</title><source>SpringerLink Journals - AutoHoldings</source><creator>Mubaid, Firas ; Kaufman, Daniel ; Wee, Tse-Luen ; Nguyen-Huu, Dong-Son ; Young, David ; Anghelopoulou, Maria ; Brown, Claire M.</creator><creatorcontrib>Mubaid, Firas ; Kaufman, Daniel ; Wee, Tse-Luen ; Nguyen-Huu, Dong-Son ; Young, David ; Anghelopoulou, Maria ; Brown, Claire M.</creatorcontrib><description>The process of fluorescence starts with the efficient generation of light that is required for the excitation of fluorophores. As such, light sources are a crucial component of a fluorescence microscope. Choosing the right illumination tool can not only improve the quality of experimental results, but also the microscope’s economic and environmental footprint. While arc lamps have historically proven to be a reliable light source for widefield fluorescence microscopy, solid-state light-emitting diodes (LEDs) have become the light source of choice for new fluorescence microscopy systems. In this paper, we demonstrate that LEDs have superior light stability on all timescales tested and use less electrical power than traditional light sources when used at lower power outputs. They can be readily switched on and off electronically, have a longer lifetime and they do not contain mercury, and thus are better for the environment. We demonstrate that it is important to measure light source power output during warm-up and switching, as a light source’s responsiveness (in terms of power) can be quite variable. Several general protocols for testing light source stability are presented. A detailed life cycle analysis shows that an LED light source can have a fourfold lower environmental impact when compared to a metal halide source.</description><identifier>ISSN: 0948-6143</identifier><identifier>EISSN: 1432-119X</identifier><identifier>DOI: 10.1007/s00418-019-01776-6</identifier><identifier>PMID: 30767050</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Developmental Biology ; Diodes ; Environmental impact ; Fluorophores ; Life cycles ; Light ; Light sources ; Mercury ; Microscopy ; Short Communication</subject><ispartof>Histochemistry and cell biology, 2019-04, Vol.151 (4), p.357-366</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2019</rights><rights>Histochemistry and Cell Biology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-62e0b2dad43176738d623f65614287b33c2ffcbde0a4768180abe9d7617aec763</citedby><cites>FETCH-LOGICAL-c375t-62e0b2dad43176738d623f65614287b33c2ffcbde0a4768180abe9d7617aec763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00418-019-01776-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00418-019-01776-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30767050$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mubaid, Firas</creatorcontrib><creatorcontrib>Kaufman, Daniel</creatorcontrib><creatorcontrib>Wee, Tse-Luen</creatorcontrib><creatorcontrib>Nguyen-Huu, Dong-Son</creatorcontrib><creatorcontrib>Young, David</creatorcontrib><creatorcontrib>Anghelopoulou, Maria</creatorcontrib><creatorcontrib>Brown, Claire M.</creatorcontrib><title>Fluorescence microscope light source stability</title><title>Histochemistry and cell biology</title><addtitle>Histochem Cell Biol</addtitle><addtitle>Histochem Cell Biol</addtitle><description>The process of fluorescence starts with the efficient generation of light that is required for the excitation of fluorophores. As such, light sources are a crucial component of a fluorescence microscope. Choosing the right illumination tool can not only improve the quality of experimental results, but also the microscope’s economic and environmental footprint. While arc lamps have historically proven to be a reliable light source for widefield fluorescence microscopy, solid-state light-emitting diodes (LEDs) have become the light source of choice for new fluorescence microscopy systems. In this paper, we demonstrate that LEDs have superior light stability on all timescales tested and use less electrical power than traditional light sources when used at lower power outputs. They can be readily switched on and off electronically, have a longer lifetime and they do not contain mercury, and thus are better for the environment. We demonstrate that it is important to measure light source power output during warm-up and switching, as a light source’s responsiveness (in terms of power) can be quite variable. Several general protocols for testing light source stability are presented. A detailed life cycle analysis shows that an LED light source can have a fourfold lower environmental impact when compared to a metal halide source.</description><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Developmental Biology</subject><subject>Diodes</subject><subject>Environmental impact</subject><subject>Fluorophores</subject><subject>Life cycles</subject><subject>Light</subject><subject>Light sources</subject><subject>Mercury</subject><subject>Microscopy</subject><subject>Short Communication</subject><issn>0948-6143</issn><issn>1432-119X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kE9LwzAYh4Mobk6_gAcZePHS-SZpk_Qow6kw8KLgLaRpOjv6ZybtYd_et3YqePAQAsmT3_vLQ8glhQUFkLcBIKYqApriklJE4ohMacxZRGn6dkymkMYqEngyIWchbAFokjJ2SiYcpJCQwJQsVlXfehesa6yb16X1bbDtzs2rcvPezUPbezwPncnKquz25-SkMFVwF4d9Rl5X9y_Lx2j9_PC0vFtHlsukiwRzkLHc5DGnOImrXDBeiAS7MCUzzi0rCpvlDkwshaIKTObSXAoqjbNS8Bm5GXN3vv3oXeh0XWLHqjKNa_ugGUMDoJSgiF7_QbdYusF2mmEwEwllCik2UsMHg3eF3vmyNn6vKejBph5tarSpv2zqocXVIbrPapf_PPnWhwAfgYBXzcb539n_xH4Crf9-AQ</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Mubaid, Firas</creator><creator>Kaufman, Daniel</creator><creator>Wee, Tse-Luen</creator><creator>Nguyen-Huu, Dong-Son</creator><creator>Young, David</creator><creator>Anghelopoulou, Maria</creator><creator>Brown, Claire M.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20190401</creationdate><title>Fluorescence microscope light source stability</title><author>Mubaid, Firas ; Kaufman, Daniel ; Wee, Tse-Luen ; Nguyen-Huu, Dong-Son ; Young, David ; Anghelopoulou, Maria ; Brown, Claire M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-62e0b2dad43176738d623f65614287b33c2ffcbde0a4768180abe9d7617aec763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Developmental Biology</topic><topic>Diodes</topic><topic>Environmental impact</topic><topic>Fluorophores</topic><topic>Life cycles</topic><topic>Light</topic><topic>Light sources</topic><topic>Mercury</topic><topic>Microscopy</topic><topic>Short Communication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mubaid, Firas</creatorcontrib><creatorcontrib>Kaufman, Daniel</creatorcontrib><creatorcontrib>Wee, Tse-Luen</creatorcontrib><creatorcontrib>Nguyen-Huu, Dong-Son</creatorcontrib><creatorcontrib>Young, David</creatorcontrib><creatorcontrib>Anghelopoulou, Maria</creatorcontrib><creatorcontrib>Brown, Claire M.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Histochemistry and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mubaid, Firas</au><au>Kaufman, Daniel</au><au>Wee, Tse-Luen</au><au>Nguyen-Huu, Dong-Son</au><au>Young, David</au><au>Anghelopoulou, Maria</au><au>Brown, Claire M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorescence microscope light source stability</atitle><jtitle>Histochemistry and cell biology</jtitle><stitle>Histochem Cell Biol</stitle><addtitle>Histochem Cell Biol</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>151</volume><issue>4</issue><spage>357</spage><epage>366</epage><pages>357-366</pages><issn>0948-6143</issn><eissn>1432-119X</eissn><abstract>The process of fluorescence starts with the efficient generation of light that is required for the excitation of fluorophores. As such, light sources are a crucial component of a fluorescence microscope. Choosing the right illumination tool can not only improve the quality of experimental results, but also the microscope’s economic and environmental footprint. While arc lamps have historically proven to be a reliable light source for widefield fluorescence microscopy, solid-state light-emitting diodes (LEDs) have become the light source of choice for new fluorescence microscopy systems. In this paper, we demonstrate that LEDs have superior light stability on all timescales tested and use less electrical power than traditional light sources when used at lower power outputs. They can be readily switched on and off electronically, have a longer lifetime and they do not contain mercury, and thus are better for the environment. We demonstrate that it is important to measure light source power output during warm-up and switching, as a light source’s responsiveness (in terms of power) can be quite variable. Several general protocols for testing light source stability are presented. A detailed life cycle analysis shows that an LED light source can have a fourfold lower environmental impact when compared to a metal halide source.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30767050</pmid><doi>10.1007/s00418-019-01776-6</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0948-6143 |
ispartof | Histochemistry and cell biology, 2019-04, Vol.151 (4), p.357-366 |
issn | 0948-6143 1432-119X |
language | eng |
recordid | cdi_proquest_miscellaneous_2210008861 |
source | SpringerLink Journals - AutoHoldings |
subjects | Biochemistry Biomedical and Life Sciences Biomedicine Cell Biology Developmental Biology Diodes Environmental impact Fluorophores Life cycles Light Light sources Mercury Microscopy Short Communication |
title | Fluorescence microscope light source stability |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T09%3A05%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Fluorescence%20microscope%20light%20source%20stability&rft.jtitle=Histochemistry%20and%20cell%20biology&rft.au=Mubaid,%20Firas&rft.date=2019-04-01&rft.volume=151&rft.issue=4&rft.spage=357&rft.epage=366&rft.pages=357-366&rft.issn=0948-6143&rft.eissn=1432-119X&rft_id=info:doi/10.1007/s00418-019-01776-6&rft_dat=%3Cproquest_cross%3E2180265128%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2180265128&rft_id=info:pmid/30767050&rfr_iscdi=true |