
Overview | ![]() PrinterFriendlyVersion |
Ex/Em(nm) | 565/779 |
MW | N/A |
CAS# | N/A |
Solvent | Water |
Storage | R/D/L |
Category | Protein-BasedTags Phycoproteins |
Related | ProteinDyes |
Spectrum | AdvancedSpectrumViewer |

- Pre-activateAntibodywithBuccutite™MTA
- ReconstituteBuccutite™MTAinDMSOat~10mg/mL.
Note:PleasestoreunusedMTAat-20°Candcouldbeuseduptotwofreezeandthawcycles. - Preparetargetantibody(Ab)inpH=8.5~9.0bufferatconcentrationabove1mg/ml
- AddtheMTAtoAbsolutionattheratioof8~10µgMTA/100µgAb.
- MixwellandreactatRTfor60minutes,rotatingduringthereaction.
- PurifythereactionmixturewithdesaltingcolumntoremoveunreactedMTAandexchangebuffertoPBSorbufferofyourchoice.
- CollecttheMTA-activatedAb,andestimatetheconcentrationby70%yieldoftheoriginalstartingamount.
- ReconstituteBuccutite™MTAinDMSOat~10mg/mL.
- ConjugatewithPre-activatedPE,PE-iFluors,orPE-iFluorTandems
- Reconstitutepre-activatedPE,PE,PE-iFluors,orPE-iFluorTandemsin100µLddH2Oto10mg/mL.
Note:Reconstitutedpre-activatedPE,PE-iFluors,orPE-iFluorTandemsarenotstableandcouldbestoredat4°Cforonemonth,pleasekeptitfromlight. - Addpre-activatedPE,PE-iFluors,orPE-iFluorTandemsdirectlytoMTA-activatedtargetAbsolution(from1.5)attheratioof300µgPE-iFluor647/100µgMTA-activatedAb.
- Rotatethemixturefor1~2hoursatroomtemperature
- TheAb/PE,PE-iFluors,orPE-iFluorTandemsconjugatesarenowreadytouse.
Optional:Ab/PE,PE-iFluors,orPE-iFluorTandemsconjugatecouldbefurtherpurifiedthroughsizeexclusionchromatographytogetbestperformance.
Note1:Theantibodyconjugateshouldbestoredat>0.5mg/mLinthepresenceofacarrierprotein(e.g.,0.1%bovineserumalbumin)and0.02-0.05%sodiumazide.
Note2:TheAb/PE,PE-iFluors,orPE-iFluorTandemsconjugatesolutioncouldbestoredat4°Cfortwomonthsandkeptfromlight.
- Reconstitutepre-activatedPE,PE,PE-iFluors,orPE-iFluorTandemsin100µLddH2Oto10mg/mL.
References&Citations | ![]() PrinterFriendlyVersion |
1. ZhaoKH,SuP,LiJ,TuJM,ZhouM,BubenzerC,ScheerH.(2006)Chromophoreattachmenttophycobiliproteinbeta-subunits:phycocyanobilin:cysteine-beta84phycobiliproteinlyaseactivityofCpeS-likeproteinfromAnabaenaSp.PCC7120.JBiolChem,281,8573.
2. PetrasekZ,SchmittFJ,TheissC,HuyerJ,ChenM,LarkumA,EichlerHJ,KemnitzK,EckertHJ.(2005)ExcitationenergytransferfromphycobiliproteintochlorophylldinintactcellsofAcaryochlorismarinastudiedbytime-andwavelength-resolvedfluorescencespectroscopy.PhotochemPhotobiolSci,4,1016.
3. LoosD,CotletM,DeSchryverF,HabuchiS,HofkensJ.(2004)Single-moleculespectroscopyselectivelyprobesdonorandacceptorchromophoresinthephycobiliproteinallophycocyanin.BiophysJ,87,2598.
4. PrasannaR,PrasannaBM,MohammadiSA,SinghPK.(2003)EvaluationofTolypothrixgermplasmforphycobiliproteincontent.FoliaMicrobiol(Praha),48,59.
5. PrasannaR,DharDW,DominicTK,TiwariON,SinghPK.(2003)IsolationandcharacterisationofphycobiliproteinrichmutantofcyanobacteriumSynechocystissp.ActaBiolHung,54,113.
6. WuP.(2000)[Phycobiliproteinandfluorescenceimmunologicalassay].ShengLiKeXueJinZhan,31,82.
7. NoubirS,LuqueI,OchoadeAldaJA,PerewoskaI,TandeaudeMarsacN,CobleyJG,HoumardJ.(2002)Co-ordinatedexpressionofphycobiliproteinoperonsinthechromaticallyadaptingcyanobacteriumCalothrixPCC7601:aroleforRcaDandRcaG.MolMicrobiol,43,749.
8. TingCS,RocapG,KingJ,ChisholmSW.(2001)PhycobiliproteingenesofthemarinephotosyntheticprokaryoteProchlorococcus:evidenceforrapidevolutionofgeneticheterogeneity.MicroBIOLOGy,147,3171.
9. TriantafilouK,TriantafilouM,WilsonKM.(2000)Phycobiliprotein-Fabconjugatesasprobesforsingleparticlefluorescenceimaging.Cytometry,41,226.
10. ZhaoKH,DengMG,ZhengM,ZhouM,ParbelA,StorfM,MeyerM,StrohmannB,ScheerH.(2000)Novelactivityofaphycobiliproteinlyase:boththeattachmentofphycocyanobilinandtheisomerizationtophycoviolobilinarecatalyzedbytheproteinsPecEandPecFencodedbythephycoerythrocyaninoperon.FEBSLett,469,9.
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然后是碱性荧光染料,造纸厂用来增加纸的亮度。
直接和分散的荧光黄,印染厂用来增加棉质和化纤面料的艳度
For principle,look at this site:
碘化丙啶(propiolium iodide,PI)能嵌入DNA双螺旋中,可使荧光强度增加约20倍,以488nm波长激发,DNA/PI复合物最大的发射波长约为615nm.
1.小鼠Lewis肺癌细胞DNA含量测定方法
(1).从C57BL/6小鼠上切除肿块,在培养皿内用PBS冲洗.
(2).去除结缔组织及脂肪,剪碎肿块.
(3).小碎片移入1.20×38mm注射针,加压使其通过,于4℃条件下重悬细胞于HBSS中.
(4).将200~300μL细胞悬液(5×105细胞/mL)中加入3mL PI(50μg/mL),染色3LL细胞,于4℃存放20~30分钟.
(5).测定580~750nm之间的发射荧光,以去除末结合PI产生的激发光与发射光谱线之间的重叠部分.
是欢快活泼的光辉色彩,是暖色系中最温暖的色,它使人联想到金色的秋天,丰硕的果实;
是一种富足、快乐而幸福的颜色。让人感觉成一种稳重、含蓄又明快的温暖;
橙色也会带来一种甜甜的感觉。

