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Crosslinkers

EDC - Thermo Scientific - 77149

EDC - Thermo Scientific - 77149

(77149)

Marca:  Thermo Scientific  | 

Embalagem:  10 MG

Prazo de Entrega: 30-45 dias corridos

mais informações

EDC - Thermo Scientific - 77149

(77149)

Marca:  Thermo Scientific  | 

Embalagem:  10 MG

Prazo de Entrega: 30-45 dias corridos

mais informações

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Descrição do Produto

EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride)


Thermo Scientific Pierce EDC is a water-soluble carbodiimide crosslinker that activates carboxyl groups for spontaneous reaction with primary amines, enabling peptide immobilization and hapten-carrier protein conjugation.

Characteristics of EDC:

• Reactive groupcarbodiimide
• Reaction target: activates carboxyl groups to conjugate to amino groups (primary amines)
• Several conjugation strategies—react EDC alone with target groups or include NHS orSulfo-NHS to increase reaction efficiency or to stabilize active intermediate for later reaction to amines
• Neutral linkage—forms neutral amide bonds between carboxyls and amines
• Water-soluble reagent—add directly to reactions in aqueous, physiological buffers
• Soluble reaction byproducts—easily removed by washing with water or dilute acid
• High-purity, crystalline reagent—use to create high-quality, activated derivatives

Properties of EDC
• Molecular formula: C8H17N3·HCl
• Molecular weight: 191.7
• Spacer arm length: 0 Å
• CAS Number: 25952-53-8
• Reactive groups: carbodiimide
• Reactivity: Forms active intermediate with carboxyl groups at pH 4.7–6.0 (optimum), then intermediate reacts with primary amines

1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC or EDAC) is a zero-length crosslinking agent used to couple carboxyl groups to primary amines. This crosslinker has been used in diverse applications such as forming amide bonds in peptide synthesis, attaching haptens to carrier proteins to form immunogens, labeling nucleic acids through 5' phosphate groups and creating amine-reactive NHS-esters of biomolecules. EDC reacts with a carboxyl to form an amine-reactive O-acylisourea intermediate. If this intermediate does not encounter an amine, it will hydrolyze and regenerate the carboxyl group. In the presence of N-hydroxysulfosuccinimide (Sulfo-NHS), EDC can be used to convert carboxyl groups to amine-reactive Sulfo-NHS esters. This is accomplished by mixing the EDC with a carboxyl containing molecule and adding Sulfo-NHS.

Applications:
• Conjugate carboxyl and amino groups among peptides and proteins
• Couple haptens to immunogenic carrier proteins (e.g., attach a peptide to KLH)
• Immobilize peptide antigens to affinity-purify antibodies
• Create NHS-activated, amine-reactive labeling compounds
• Crosslink proteins to carboxyl coated beads or surfaces
• Activate nanoparticles with amine-reactive Sulfo-NHS esters
• DNA labeling through 5' phosphate groups (see Tech Tip #30)

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