Analytical Behavior of Fura-2 and Its Determination of [Ca^2+ ]i in Lymphocytes Treated with Cefotaxime
The interaction of Fura-2 with Ca^2+ is studied using steady fluorescence technique. The effect of pH on the spectra behavior of Fura-2 in the presence of Ca^2+ is investigated, the excitation maxima (340 nm) and the isobestic point (360 nm) for the fluorescence spectra of Fura-2 depend on pH. At di...
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Veröffentlicht in: | 测试科学与仪器 2010, Vol.1 (4), p.395-400 |
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creator | 双少敏 乔晓娜 王丹丹 樊丽 芦冬涛 慕丽晓 周叶红 |
description | The interaction of Fura-2 with Ca^2+ is studied using steady fluorescence technique. The effect of pH on the spectra behavior of Fura-2 in the presence of Ca^2+ is investigated, the excitation maxima (340 nm) and the isobestic point (360 nm) for the fluorescence spectra of Fura-2 depend on pH. At different temperatures the apparent dissociation constants ( Kd ) of Fura-2-Ca^2+ complex are examined, Kd is found to decrease with increasing temperatures (20 ℃, 37 ℃, 50 ℃ ) and △His calculated to be 21.16 kJ/mol by using the Van' t Hoff equation at pH 7.4 for all the temperatures tested. The determination of intracellular Ca^2+ concentration ( [Ca^2+ ] i ) in lymphocyte is developed by using Fura-2 as a fluorescence probe in the presence of Cefotaxime at 37 ℃ and pH 7.4. |
doi_str_mv | 10.3969/j.issn.1674-8042.2010.04.21 |
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The effect of pH on the spectra behavior of Fura-2 in the presence of Ca^2+ is investigated, the excitation maxima (340 nm) and the isobestic point (360 nm) for the fluorescence spectra of Fura-2 depend on pH. At different temperatures the apparent dissociation constants ( Kd ) of Fura-2-Ca^2+ complex are examined, Kd is found to decrease with increasing temperatures (20 ℃, 37 ℃, 50 ℃ ) and △His calculated to be 21.16 kJ/mol by using the Van' t Hoff equation at pH 7.4 for all the temperatures tested. The determination of intracellular Ca^2+ concentration ( [Ca^2+ ] i ) in lymphocyte is developed by using Fura-2 as a fluorescence probe in the presence of Cefotaxime at 37 ℃ and pH 7.4.</description><identifier>ISSN: 1674-8042</identifier><identifier>DOI: 10.3969/j.issn.1674-8042.2010.04.21</identifier><language>eng</language><publisher>School of Chemistry and Chemical Engineering,Shanxi University,Taiyuan 030006,China%China Research Institute of Daily Chemical Industry,Taiyuan 030006,China</publisher><subject>pH值 ; 光谱行为 ; 头孢噻肟钠 ; 淋巴细胞 ; 温度上升</subject><ispartof>测试科学与仪器, 2010, Vol.1 (4), p.395-400</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1181-ad83454e075294e42f652ca2145dcb6c4a16430b82e52f075931355fafb3af263</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/70833X/70833X.jpg</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids></links><search><creatorcontrib>双少敏 乔晓娜 王丹丹 樊丽 芦冬涛 慕丽晓 周叶红</creatorcontrib><title>Analytical Behavior of Fura-2 and Its Determination of [Ca^2+ ]i in Lymphocytes Treated with Cefotaxime</title><title>测试科学与仪器</title><addtitle>Journal of Measurement Science and Instrumentation</addtitle><description>The interaction of Fura-2 with Ca^2+ is studied using steady fluorescence technique. The effect of pH on the spectra behavior of Fura-2 in the presence of Ca^2+ is investigated, the excitation maxima (340 nm) and the isobestic point (360 nm) for the fluorescence spectra of Fura-2 depend on pH. At different temperatures the apparent dissociation constants ( Kd ) of Fura-2-Ca^2+ complex are examined, Kd is found to decrease with increasing temperatures (20 ℃, 37 ℃, 50 ℃ ) and △His calculated to be 21.16 kJ/mol by using the Van' t Hoff equation at pH 7.4 for all the temperatures tested. The determination of intracellular Ca^2+ concentration ( [Ca^2+ ] i ) in lymphocyte is developed by using Fura-2 as a fluorescence probe in the presence of Cefotaxime at 37 ℃ and pH 7.4.</description><subject>pH值</subject><subject>光谱行为</subject><subject>头孢噻肟钠</subject><subject>淋巴细胞</subject><subject>温度上升</subject><issn>1674-8042</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNo9kM1OwkAcxPegiQR5h41evLTuZz-OWEVJSLzgySj5d7tLF8pWukXoM_hKvpOvYAnG0yQzv0wyg9A1JSFPo_R2FVrvXUijWAQJESxkpI-ICBk9Q4N_-wKNvLc5ITJJYxnzAbJjB1XXWgUVvtMlfNq6wbXBk10DAcPgCjxtPb7XrW421kFra3fMXzN4Zz_fX_jNYuvwrNt8lLXqWu3xvNHQ6gLvbVviTJu6hYPd6Et0bqDyevSnQ_QyeZhnT8Hs-XGajWeBojShARQJF1JoEkuWCi2YiSRTwKiQhcojJYBGgpM8YVoy01Mpp1xKAybnYFjEh-jm1LsHZ8AtF6t61_Qj_UL59aHrtsdriCCM9ujVCVVl7ZZb28M5qLWxlV5wKRiPKOG_ZYVoww</recordid><startdate>2010</startdate><enddate>2010</enddate><creator>双少敏 乔晓娜 王丹丹 樊丽 芦冬涛 慕丽晓 周叶红</creator><general>School of Chemistry and Chemical Engineering,Shanxi University,Taiyuan 030006,China%China Research Institute of Daily Chemical Industry,Taiyuan 030006,China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>~WA</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>2010</creationdate><title>Analytical Behavior of Fura-2 and Its Determination of [Ca^2+ ]i in Lymphocytes Treated with Cefotaxime</title><author>双少敏 乔晓娜 王丹丹 樊丽 芦冬涛 慕丽晓 周叶红</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1181-ad83454e075294e42f652ca2145dcb6c4a16430b82e52f075931355fafb3af263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>pH值</topic><topic>光谱行为</topic><topic>头孢噻肟钠</topic><topic>淋巴细胞</topic><topic>温度上升</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>双少敏 乔晓娜 王丹丹 樊丽 芦冬涛 慕丽晓 周叶红</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-自然科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>测试科学与仪器</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>双少敏 乔晓娜 王丹丹 樊丽 芦冬涛 慕丽晓 周叶红</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analytical Behavior of Fura-2 and Its Determination of [Ca^2+ ]i in Lymphocytes Treated with Cefotaxime</atitle><jtitle>测试科学与仪器</jtitle><addtitle>Journal of Measurement Science and Instrumentation</addtitle><date>2010</date><risdate>2010</risdate><volume>1</volume><issue>4</issue><spage>395</spage><epage>400</epage><pages>395-400</pages><issn>1674-8042</issn><abstract>The interaction of Fura-2 with Ca^2+ is studied using steady fluorescence technique. The effect of pH on the spectra behavior of Fura-2 in the presence of Ca^2+ is investigated, the excitation maxima (340 nm) and the isobestic point (360 nm) for the fluorescence spectra of Fura-2 depend on pH. At different temperatures the apparent dissociation constants ( Kd ) of Fura-2-Ca^2+ complex are examined, Kd is found to decrease with increasing temperatures (20 ℃, 37 ℃, 50 ℃ ) and △His calculated to be 21.16 kJ/mol by using the Van' t Hoff equation at pH 7.4 for all the temperatures tested. The determination of intracellular Ca^2+ concentration ( [Ca^2+ ] i ) in lymphocyte is developed by using Fura-2 as a fluorescence probe in the presence of Cefotaxime at 37 ℃ and pH 7.4.</abstract><pub>School of Chemistry and Chemical Engineering,Shanxi University,Taiyuan 030006,China%China Research Institute of Daily Chemical Industry,Taiyuan 030006,China</pub><doi>10.3969/j.issn.1674-8042.2010.04.21</doi><tpages>6</tpages></addata></record> |
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subjects | pH值 光谱行为 头孢噻肟钠 淋巴细胞 温度上升 |
title | Analytical Behavior of Fura-2 and Its Determination of [Ca^2+ ]i in Lymphocytes Treated with Cefotaxime |
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