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產(chǎn)品名稱

Biotinyl-phenylboronic acid

產(chǎn)品貨號(hào)

Axon 2256 CAS [N.A.] MF C16H22BN3O4SMW 363.24 Purity: 99% Soluble in 0.1N NaOH(aq), MeOH and DMSO Description Biotin functionalized arylboronic acid for the use of palladium-catalyzed oxidative Heck reaction to protein-bound alkenes and Suzuki-Miyaura cross-coupling for labeling of protein bound phenylhalides in high yields and with excellent chemoselectivity. Reagent for bio-orthogonal protein-ligation. Signal enhancement with streptavidin-HRP.*Sold in collaboration with RuG (University of Groningen)? References Certificates Categories Extra info ME Ourailidou et al. Aqueous oxidative Heck reaction as a protein-labeling strategy. Chembiochem. 2014, 15, 209-212. ? F D'Hooge et al. Biotinylated boronic acid fluorophore conjugates: Quencher elimination strategy for imaging and saccharide detection. RSC Adv. 2012, 2, 3274-3280. ? Chalker et al. A Convenient Catalyst for Aqueous and Protein Suzuki-Miyaura Cross-Coupling J. Am. Chem. Soc. 2009, 131, 16346-16347 ? C.D. Spicer et al. Palladium-mediated site-selective Suzuki-Miyaura protein modification at genetically encoded aryl halides. Chem. Commun. 2011, 47, 1698-700 ? C.D. Spicer et al. Palladium-mediated cell-surface labeling. J. Am. Chem. Soc. 2012, 134(2), 800-3. Certificate of Analysis Material Safety Data Sheet Miscellaneous Proteins RuG Collaboration Products Biotinylated arylboronic acid for bio-orthogonal chemistry Chemical name 3-(5-(2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)phenylboronic acid Source information Sold in collaboration with RuG (University of Groningen) Parent CAS No. [N.A.] Order Size Unit Price Stock 5 mg €95.00 In Stock

產(chǎn)品價(jià)格

現(xiàn)貨詢價(jià)，電話：010-67529703

產(chǎn)品規(guī)格

產(chǎn)品品牌

axonmedchem

產(chǎn)品概述

產(chǎn)品詳情

Biotinyl-phenylboronic acid

Based on 8 reference(s) in Google Scholar 9 10 8

Axon 2256

CAS [N.A.]

MF C16H22BN3O4S
MW 363.24

Purity: 99%
Soluble in 0.1N NaOH(aq), MeOH and DMSO

Biotinyl-phenylboronic acid

Description

Biotin functionalized arylboronic acid for the use of palladium-catalyzed oxidative Heck reaction to protein-bound alkenes and Suzuki-Miyaura cross-coupling for labeling of protein bound phenylhalides in high yields and with excellent chemoselectivity. Reagent for bio-orthogonal protein-ligation. Signal enhancement with streptavidin-HRP.
*Sold in collaboration with RuG (University of Groningen)?

ME Ourailidou et al. Aqueous oxidative Heck reaction as a protein-labeling strategy. Chembiochem. 2014, 15, 209-212.

F D'Hooge et al. Biotinylated boronic acid fluorophore conjugates: Quencher elimination strategy for imaging and saccharide detection. RSC Adv. 2012, 2, 3274-3280.

Chalker et al. A Convenient Catalyst for Aqueous and Protein Suzuki-Miyaura Cross-Coupling J. Am. Chem. Soc. 2009, 131, 16346-16347

C.D. Spicer et al. Palladium-mediated site-selective Suzuki-Miyaura protein modification at genetically encoded aryl halides. Chem. Commun. 2011, 47, 1698-700

C.D. Spicer et al. Palladium-mediated cell-surface labeling. J. Am. Chem. Soc. 2012, 134(2), 800-3.

Certificate of Analysis
Material Safety Data Sheet

Miscellaneous Proteins RuG Collaboration Products

Biotinylated arylboronic acid for bio-orthogonal chemistry

Chemical name

3-(5-(2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)phenylboronic acid

Source information

Sold in collaboration with RuG (University of Groningen)

Parent CAS No.

[N.A.]

產(chǎn)品資料

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