Hledali jste: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide+methiodide

Dodavatel: Thermo Scientific

Popis: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide 98%

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Dodavatel: Thermo Scientific

Popis: Appearance: White to off-white Crystalline powder

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Dodavatel: Apollo Scientific

Popis: EDC (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide) 98%

Dodavatel: Apollo Scientific

Popis: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

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Dodavatel: Apollo Scientific

Popis: EDAC is a water soluble condensing reagent.

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Dodavatel: Thermo Scientific

Popis: EDC (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide) 97%

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Dodavatel: Thermo Scientific

Popis: EDC (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide) 98%

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Katalogové číslo: (59002.)

Dodavatel: Biotium

Popis: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

Měrná jednotka: 1 * 100 mg

Akce

Dodavatel: Thermo Scientific

Popis: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) 98+%

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Dodavatel: Thermo Scientific

Popis: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) 98+%

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Dodavatel: G-Biosciences

Popis: EDC is a heterobifunctional, water-soluble, zero-length carbodiimide crosslinker that is used to couple carboxyl groups to primary amines. EDC activates carboxyl groups first and forms amine reactive O-acylisourea imtermediate that spontaneously reacts with primary amines to form an amide bond and isourea by-product.

Dodavatel: Merck

Popis: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Dodavatel: Merck

Popis: EDC (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide), Sigma-Aldrich®

Dodavatel: Merck

Popis: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Dodavatel: Merck

Popis: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

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Dodavatel: Thermo Fisher Scientific

Popis: Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.