Thermo Fisher Scientific EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride), 5 g
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
22981 | - | Thermo Fisher Scientific 22981 EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride), 25 g Each pk | 재고문의 | pk | 605,000원 | - | 665,500원 | |
A35391 | - | Thermo Fisher Scientific A35391 Pierce EDC, No-Weigh Format, 10 x 1 mg Each pk | 재고문의 | pk | 251,000원 | - | 276,100원 | |
22980 | - | Thermo Fisher Scientific 22980 EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride), 5 g Each pk | 재고문의 | pk | 202,000원 | - | 222,200원 | |
77149 | - | Thermo Fisher Scientific 77149 EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride), 10 mg Each pk | 재고문의 | pk | 105,000원 | - | 115,500원 |
다른 상품 둘러보기
Thermo Scientific™
Pierce™ EDC, No-Weigh™ Format
Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms자세히 알아보기
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.
Thermo Scientific No-Weigh products are specialty reagents provided in a pre-aliquoted format. The pre-weighed packaging prevents the loss of reagent reactivity and contamination over time by eliminating the repetitive opening and closing of the vial. The format enables use of a fresh vial of reagent each time, eliminating the hassle of weighing small amounts of reagents and reducing concerns over reagent stability.
Characteristics of EDC:
• Reactive group: carbodiimide
• Reaction target: activates carboxyl groups to conjugate to amino groups (primary amines)
• Several conjugation strategies—react EDC alone with target groups or include NHS or Sulfo-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)
Product References:
Crosslinker Application Guide -- search for recent literature references for this product
사양
화학물질 반응성Amine-Carboxyl
CleavableNo
설명EDC
분자량191.7
페길레이티드No
스페이서 암 길이0.0 Å
세포 투과성No
배송 조건Wet Ice
제품라인Pierce™
라벨링 방법Chemical Labeling
교차결합제 유형Heterobifunctional
반응성 부분Carbodiimide
스페이서Short (<10 Å)
형태Powder
수량5 g
용해도Water
형식Standard, Single-use, Premium-grade
수용성Yes
제품 유형Crosslinker
Unit SizeEach
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