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ID:11568252
大小:94.00 KB
页数:5页
时间:2018-07-12
《与氨基反应的荧光探针》由会员上传分享,免费在线阅读,更多相关内容在行业资料-天天文库。
1、与氨基反应的荧光探针HighlightsofRhodamineandTRITCLabelingKits:·Fast–labelandpurifyantibodyinaboutonehour·Amine-specificlabeling–theNHS-esterorisothiocyanateefficientlylabelsantibodiesandotherpurifiedproteinsatprimaryamines(lysinesidechains)·Optimizedprocedure–followingthestandardprotoc
2、olresultsinantibodieswithexcellentdye:proteinratiosforoptimumactivityandfluorescence·Single-usefluors–noneedtoweightinyamountspowder;kitscontainsingle-usevialsofreagent·Efficientpurification–kitsincludepurificationresinandeasy-to-usespincolumns,ensuringrapidandefficientremova
3、lofnon-reacteddyeandexcellentproteinrecoveryApplicationsforRhodamineLabelingReagents:·Labelantibodiesforuseasimmunofluorescentprobes·Labeloligonucleotidesforhybridizationprobes·DetectproteinsingelsandonWesternblotsPropertiesofRhodamineDyes:ThermoScientificPierceRhodamineDyesa
4、remixturesofisomerswithreactivegroupsattachedatthe5-and6-positionsofthebottomring.Thepropertiesoftheseisomersareindistinguishableintermsofexcitationandemissionspectra,andforproteinapplicationsthereisnoneedtoisolateaspecificisomer.TRITCisthebasetetramethylrhodaminemoleculefunc
5、tionalizedwithanisothiocyanatereactivegroup(–N=C=S)atoneoftwohydrogenatomsonthebottomringofthestructure.Thisderivativeisreactivetowardsprimaryaminegroupsonproteins,peptidesandotherbiomolecules.NHS-RhodamineisactivatedwiththeN-hydroxy-succinimidyl-ester(NHSester)functionalgrou
6、p.ComparedtoTRITC,theNHS-esterderiviativehasgreaterspecificitytowardprimaryaminesinthepresenceofothernucleophilesandresultsinamorestablelinkagefollowinglabeling.TexasRed*SulfonylChlorideisalong-wavelengthderivativeofrhodaminethatismodifiedwithsulfonylchlorideforreactiontoprim
7、aryamines.WerecommendDyLight594NHSEsterasanalternativetoTexasRedSulfonylChloridebecauseitisbrighter,morephotostableandhasamorespecificlabelingchemistrythatcanbeusedatphysiologicpH.AMCA(aminomethylcoumarinacetate)isabluefluorescentdyewhosereactivederivativesareusedascontrastin
8、gprobesfordoubleandtriplelabelinginimmunofluorescencemicroscopy,arra
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