(Suc-LLVY)2-Rhodamineisafluorogenicsubstrateforthechymotrypsin–likeactivityofthe20Sand26Sproteasomes.Workingconcentrationsofthissubstrateis20-100µM.ThereleasedRhodamine110fluorescencecanbedetectedbyafluorimeterorplatereaderatexcitation/emissionof495nm/520nm,respectively.ComparedtoAMC,Rhodamine110isexcitedatlongerwavelengththatcansignificantlyenhancethesignal/noiseratio.ThissubstrateisextremlyvaluableforscreeningsmallchemicalinhibitorsofproteasomesbyavoidingtheinterferencefromchemicalcompoundautofluorescencethatoftenoccursatshorterwavelengthsaroundUVornear-UVregions.
Whenusedtodetermineproteasomeactivityincelllysates,celllysatesthatarepre-treatedwithaproteasomeinhibitorsuchasMG132,PS341orepoxomicincanbeusedtodeterminethefluorescencecontributedbyothercellularproteasesthatcleavethissubstrate.Re
ADIngsfromproteasomeinhibitor-treatedlysatesshouldbesubtracted.
| ProductName: | (Suc-Leu-Leu-Val-Tyr)2-Rhodamine110 |
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| AlsoKnownAs: | (Suc-LLVY)2-Rhodamine110 |
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| CatalogNo.: | G1111 |
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| Size: | 10mg |
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| MolecularWeight: | 1507.7Da |
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| Species: | N/A |
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| Source: | Synthetic |
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| Stock: | Powder |
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| Concentration: | N/A |
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| QualityAssurance: | >98%byHPLCandNMR |
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| Storage: | EligIBLeforroomtemperatureshipping.Storeat-80°Cuponreceiving;avoidmultiplefreeze-thawcyclesafterdissolvinginDMSO. |
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| PDFDataSheet: | DownloadPDFdatasheet,MSDS |
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| NCBIRefSeq: | N/A |
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| Image(s): | No |
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| ShippingMethod: | Roomtemperatureshipping |
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| References: | No |
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Details
(Suc-LLVY)2-Rhodamineisafluorogenicsubstrateforthechymotrypsin–likeactivityofthe20Sand26Sproteasomes.Theworkingconcentrationofthissubstrateis20-100µM.ThereleasedRhodamine110fluorescencecanbedetectedbyafluorimeterorplatereaderatexcitation/emissionwavelengthsof495nm/520nm,respectively.ComparedtoAMC,rhodamine110isexcitedatlongerwavelengththatcansignificantlyenhancethesignal/noiseratio.ThissubstrateisextremlyvaluableforscreeningsmallchemicalinhibitorsofproteasomesbyavoidingtheinterferencefromchemicalcompoundautofluorescencethatoftenoccursatshorterwavelengthsaroundUVornear-UVregions.Whenusedtodetermineproteasomeactivityincelllysates,celllysatesthatarepre-treatedwithaproteasomeinhibitorsuchasMG132,PS341orepoxomicinshouldbeusedtodeterminethefluorescencecontributedbyothercellularproteasesthatcleavethissubstrate.Readingsfromproteasomeinhibitor-treatedlysatescanbesubtractedasbackground.
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