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当前位置: 首页 > 产品中心 > Other_biological_dyes > AAT Bioquest/Calbryte™590 AM/20700/2x50 ug
商品详细AAT Bioquest/Calbryte™590 AM/20700/2x50 ug
AAT Bioquest/Calbryte™590 AM/20700/2x50 ug
AAT Bioquest/Calbryte™590 AM/20700/2x50 ug
商品编号: 20700
品牌: aatbio
市场价: ¥56560.00
美元价: 33936.00
产地: 美国(厂家直采)
公司:
产品分类: 其他生物染料
公司分类: Other_biological_dyes
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Overview
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Ex/Em(nm)573/588
MW1218.77
CAS#N/A
SolventDMSO
StorageF/D/L
CategoryGPCR
CalciumGPCRAssays
RelatedCalciumChannels
pHandIonIndicators
TheintracellularcalciumfluxassayisawidelyusedmethodinmonitoringsignaltransductionpathwaysandhighthroughputscreeningofGprotein–coupledreceptors(GPCRs)andcalciumchanneltargets.FollowedbyRhod-2beingintroducedin1989,Rhod-4andCal-590werelaterdevelopedwithimprovedsignal/backgroundratio,andtheybecamethewidelyusedredfluorescentCa2+indicatorsforconfocalmicroscopy,flowcytometryandhighthroughputscreeningapplications.InCHOandHEKcellsRhod-4andCal-590havecellularcalciumresponsethatare10timesmoresensitivethanRhod-2AM.However,Cal-590andRhod-4arestilllesssensitivetocalciumincellsthanthecorrespondinggreenfluorescentcalciumindicators(e.g.,Fluo-8andCal-520).Calbryte™590isanewgenerationofredfluorescentindicatorsforthemeasurementofintracellularcalcium.Itsgreatlyimprovedsignal/backgroundratioandintracellularretentionpropertiesmakeCalbryte™590AMthemostrobustredfluorescentindicatorforevaluatingGPCRandcalciumchanneltargetsaswellasforscreeningtheiragoNISTsandantagonistsinlivecells.LikeotherdyeAMcellloADIng,Calbryte™590AMesterisnon-fluorescentandoncegetsinsidethecell,itishydrolyzedbyintracellularesteraseandgetsactivated.Theactivatedindicatorisapolarmoleculethatisnolongercapableoffreelydiffusingthroughcellmembrane,essentiallytrappedinsidecells.
SpectrumAdvancedSpectrumViewer

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Thisprotocolonlyprovidesaguideline,andshouldbemodifiedaccordingtoyourspecificneeds.
  1. LoadCellswithCalbryte™520,Calbryte™590orCalbryte™630AMEsters:
    Calbryte™AMestersshouldbereconstitutedjustbeforeuseinanhydrousDMSO.TheDMSOstocksolutionsmaybestored(desiccated)at–20°Candprotectedfromlight.Undertheseconditions,AMestersshouldbestableforthreemonths.FollowingisourrecommendedprotocolforloadingCalbryte™520AM,Calbryte™590AMorCalbryte™630AMestersintolivecells.Thisprotocolonlyprovidesaguideline,andshouldbemodifiedaccordingtoyourspecificneeds.

    1. Preparea2to5mMstocksolutionofCalbryte™520AM,Calbryte™590AMorCalbryte™630AMestersinanhydrousDMSO.
    2. DissolveCalbryte™520AM,Calbryte™590AMorCalbryte™630AMinDMSOorthawanaliquotoftheindicatorstocksolutiontoroomtemperature.Prepareadyeworkingsolutionof10to20µMinHanksandHepesbuffer(HHBS)orthebufferofyourchoicewith0.04%Pluronic®F-127.Theexactconcentrationoftheindicatorrequiredforcellloadingmustbedeterminedempirically.
      Note:ThenonionicdetergentPluronic®F-127issometimesusedtoincreasetheaqueoussolubilityofCalbryte™520AM,Calbryte™590AMorCalbryte™630AMesters.AvarietyofPluronic®F-127solutionscanbepurchasedfromAATBioquest.
    3. Ifyourcells(suchasCHOcells)containorganicanion-transports,probenecid(1-2mM)maybeaddedtothedyeworkingsolution(finalinwellconcentrationwillbe0.5-1mM)toreduceleakageofthede-esterifiedindicators.ProbenecidmightnotbeneededeveninCHOcellswithCalbryte™520AM
      Note:AvarietyofReadiUse™probenecidincludingwatersolublesodiumsaltandstABIlizedsolutioncanbepurchasedfromAATBioquest.
    4. Addequalvolumeofthedyeworkingsolution(fromStepborc)intoyourcellplate.
    5. Incubatethedye-loadingplateinacellincubatorfor~60minutes,andthenincubatetheplateatroomtemperatureforanother15minutes.
    6. ReplacethedyeworkingsolutionwithHHBSorabufferofyourchoicethatcontainsananiontransporterinhibitor,suchas1mMprobenecid,toremoveexcessprobes.
    7. RunthecalciumtestsatEx/Em=490/525nmforCalbryte™520AM,540/590nmforCalbryte™590AMor610/640nmforCalbryte™630AM.
References&Citations
CitationExplorer

CalreticulinregulatesTGF-β1-inducedepithelialmesenchymaltransitionthroughmodulatingSmadsignalingandcalciumsignaling
Authors:YanjiaoWu,XiaoliXu,LunkunMa,QianYi,WeichaoSun,LilingTang
Journal:TheInternationalJournalofBiochemistry&CellBIOLOGy(2017)

Dexmedetomidinereduceshypoxia/reoxygenationinjurybyregulatingmitochondrialfissioninrathippocampalneurons
Authors:JiaLiu,QingDu,HeZhu,YuLi,MaodongLiu,ShoushuiYu,ShileiWang
Journal:IntJClinExpMed(2017):6861--6868

Monosialoganglioside1mayalleviateneurotoxicityinducedbypropofolcombinedwithremifentanilinneuralstemcells
Authors:JiangLu,Xue-qinYao,XinLuo,YuWang,SookjaKimChung,He-xinTang,ChiWaiCheung,Xian-yuWang,ChenMeng,QingLi
Journal:NeuralRegenerationResearch(2017):945

Obtainingspontaneouslybeatingcardiomyocyte-likecellsfromadipose-derivedstromalvascularfractionsculturedonenzyme-crosslinkedgelatinhydrogels
Authors:GangYang,ZhenghuaXiao,XiaomeiRen,HaiyanLong,KunlongMa,HongQian,YingqiangGuo
Journal:ScientificReports(2017):41781

Di(2-ethylhexyl)phthalate-inducedapoptosisinratINS-1cellsisdependentonactivationofendoplasmicreticulumstressandsuppressionofantioxidantprotection
Authors:XiaSun,YiLin,QianshengHuang,JunpengShi,LingQiu,MeiKang,YajieChen,ChaoFang,TingYe,SijunDong
Journal:Journalofcellularandmolecularmedicine(2015):581--594

Theeffectofmitochondrialcalciumuniporteronmitochondrialfissioninhippocampuscellsischemia/reperfusioninjury
Authors:LantaoZhao,ShuhongLi,ShileiWang,NingYu,JiaLiu
Journal:Biochemicalandbiophysicalresearchcommunications(2015):537--542

FungusinducesthereleaseofIL-8inhumancornealepithelialcells,viaDectin-1-mediatedproteinkinaseCpathways.
Authors:Xu-DongPeng,Gui-QiuZhao,JingLin,NanJiang,QiangXu,Cheng-ChengZhu,Jain-QiuQu,LinCong,HuiLi
Journal:Internationaljournalofophthalmology(2014):441--447

Propofolandremifentanilatmoderateandhighconcentrationsaffectproliferationanddifferentiationofneuralstem/Progenitorcells
Authors:QingLi,JiangLu,XianyuWang
Journal:Neuralregenerationresearch(2014):2002

Roleofmitochondrialcalciumuniporterinregulatingmitochondrialfissioninthecerebralcortexesoflivingrats
Authors:NanLiang,PengWang,ShileiWang,ShuhongLi,YuLi,JinyingWang,MinWang
Journal:JournalofNeuralTransmission(2014):593--600

Increasedexpressionofcelladhesionmolecule1bymastcellsasacauseofenhancednerve--mastcellinteractioninahapten-inducedmousemodelofatopicdermatitis
Authors:MHagiyama,TInoue,TFuruno,TIino,SItami,MNakanishi,HAsada,YHosokawa,AIto
Journal:BritishJournalofDermatology(2013):771--778


品牌介绍
美国AAT Bioquest Inc.(前身是ABD Bioquest,Inc.)是一家为从事生命科学研究、诊断研发及药物开发的科学家研发、生产和销售生物分析研究试剂和试剂盒的公司。公司致力于光谱学检测领域,包括吸收(颜色)、荧光和发光技术。AAT Bioquest的产品帮助全世界的科学家和生物医药研究者更好的了解生物化学、免疫学、细胞生物学和分子生物学等领域。AAT Bioquest会不断研发新产品,快速地丰富各个领域的产品。 1)提供反应探针和发光探针,生物素和端粒酶能够应用于标记药物小分子和生物聚合物,如蛋白、核酸以及其他碳水化合物; 2)研究并生产荧光和发光探针用于检测蛋白,核酸和活细胞; 3)不断推出新型的荧光和发光探针用于检测多种酶,特别是检测水解酶和氧化还原酶类; 4)致力于开发用于信号转导研究的试剂; 5)提供生理和神经探针,特别是钙离子指示剂和膜电位探针。
品牌分类
淋巴细胞信号传导 GPCR抗体 羰基活性生物素 细胞代谢 胺反应生物素 链霉亲和素结合物 生物素化抗IgGs 乙酰基特异性抗体 细胞骨架抗体
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