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Thank you very much for your interest in our products. All prices listed on our website are ex-works, Germany, and may attract customs duties when imported.
You may/will be contacted by the shipping company for additional documentation that may be required by the US Customs for clearance.
We offer you the convenience of buying through a local partner, Peptide Solutions LLC who can import the shipment as well as prepay the customs duties and brokerage on your behalf and provide the convenience of a domestic sale.
Continue to Iris Biotech GmbHSend request to US distributorChemical name: N-(6-(azidomethyl)pyridin-3-yl)-15-(4,4-dimethyl-2,6-dioxocyclohexylidene)-1-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)-3,6,9,12-tetraoxa-16-azanonadecan-19-amide // Synonyms: Dde-Biotin-Picolyl-Azide, N3-Picolyl-Dde-PEG(4)-Biotin
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This cleavable trifunctional biotinylating reagent incorporating a cleavable linker is highly valuable for usage in protein enrichment. A linker based on the Dde protecting group leads to efficient release of protein targets under mild aqueous buffered conditions with 2% hydrazine. The cleaved moiety that remains on the modified peptide only minimally changes the peptide mass and generates an additional positive charge, which facilitates peptide sequencing by ETD.
Cleavable trifunctional biotin reagents for protein labelling, capture and release; Yinliang Yang and Steven H. L. Verhelst; Chem. Commun. 2013; 49: 5366-5368. DOI: 10.1039/C3CC42076K.
Comprehensive mapping of O-GlcNAc modification sites using a chemically cleavable tag; Matthew E. Griffin, Elizabeth H. Jensen, Daniel E. Mason, Courtney L. Jenkins, Shannon E. Stone, Eric C. Peters and Linda C. Hsieh-Wilson; Mol. BioSyst. 2016; 12: 1756-1759. DOI: 10.1039/C6MB00138F.
Mapping the Binding Site of BMS-708163 on γ-Secretase with Cleavable Photoprobes; Gertsik N, Am Ende CW, Geoghegan KF, Nguyen C, Mukherjee P, Mente S, Seneviratne U, Johnson DS, Li YM; Cell Chem Biol. 2017; 24(1): 3-8. DOI: 10.1016/j.chembiol.2016.12.006.
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