EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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Growing Embossed Nanostructures of Polymer Brushes on Wet-Etched Silicon Templated via Block Copolymers Chemical modification of antibodies enables the formation of stable antibody-gold nanoparticle conjugates for biosensing.

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Q36542535-D55B9B0D-FDC2-4CD8-9AED-1030EDA3744E Q47594023-F3C4FB83-C13F-462E-A4D5-14949B374D62

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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im Jahr 2015 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована у 2015

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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P1476

EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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Chuan Jiang

http://www.w3.org/2001/XMLSchema#string

Hong-Ning Zheng

http://www.w3.org/2001/XMLSchema#string

Kun Li

http://www.w3.org/2001/XMLSchema#string

Qin Yan

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Shou-Jun Xiao

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CXIX.—The formation and stability of spiro-compounds. Part I. spiro-Compounds from cyclohexane

The infrared absorption of amino acid side chains.

Succinimidyl ester surface chemistry: implications of the competition between aminolysis and hydrolysis on covalent protein immobilization.

Reaction of an Introverted Carboxylic Acid with Carbodiimide.

gem-disubstituent effect: theoretical basis and synthetic applications.

Gas-phase reactivity of carboxylic acid functional groups with carbodiimides.

Mechanism of amide formation by carbodiimide for bioconjugation in aqueous media.

Rethinking amide bond synthesis.

A tetrafluorophenyl activated ester self-assembled monolayer for the immobilization of amine-modified oligonucleotides.

Semiquantitative study of the EDC/NHS activation of acid terminal groups at modified porous silicon surfaces.

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69939-69947

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P31

scholarly article

P356

10.1039/C5RA13844B

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-01-01T00:00:00Z

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EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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P2860

P2860

EDC/NHS activation mechanism of polymethacrylic acid: anhydride versus NHS-ester

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577