EDAC, 1-Ethyl-3-(3-Dimethylaminopropyl)carbodiimide, Hydrochloride
EDAC, 1-Ethyl-3-(3-Dimethylaminopropyl)carbodiimide, Hydrochloride
Invitrogen™

EDAC, 1-Ethyl-3-(3-Dimethylaminopropyl)carbodiimide, Hydrochloride

EDAC is a water-soluble carbodiimide that can be used to crosslink biological substances that contain carboxylate acids and primary amines.Read more
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Catalog NumberQuantity
E2247100 mg
Catalog number E2247
Price (TWD)
2,890.00
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Ends: 31-Dec-2025
3,600.00
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Quantity:
100 mg
Price (TWD)
2,890.00
온라인 행사
Ends: 31-Dec-2025
3,600.00
Save 710.00 (20%)
Each
Add to cart
EDAC is a water-soluble carbodiimide that can be used to crosslink biological substances that contain carboxylate acids and primary amines. Protocols for crosslinking molecules with this reagent can be found in Bioconjugate Techniques, by G.T. Hermanson (B-7884).
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Recommended StorageStore in freezer (-5 to -30°C).
Molecular Weight (g/mol)191.7
Physical FormSolid
Quantity100 mg
Unit SizeEach

Frequently asked questions (FAQs)

Is your EDAC compound the same as your EDC compound?

Yes, both acronyms are used for the same compound. The chemical name for EDC is 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and the chemical name for EDAC is N-3-(3-dimethylaminopropyl)-N-ethyl-carbodiimide. Both of these compounds are structurally equivalent.

Citations & References (93)

Citations & References
Abstract
Tuftsin binds neuropilin-1 through a sequence similar to that encoded by exon 8 of vascular endothelial growth factor.
Authors:von Wronski MA,Raju N,Pillai R,Bogdan NJ,Marinelli ER,Nanjappan P,Ramalingam K,Arunachalam T,Eaton S,Linder KE,Yan F,Pochon S,Tweedle MF,Nunn AD
Journal:The Journal of biological chemistry
PubMed ID:16371354
Modification of the actin interface of skeletal myosin subfragment-1 by treatment with dibromobimane.
Authors:Mornet D, Ue K, Chaussepied P, Morales MF
Journal:Eur J Biochem
PubMed ID:3758077
'Recently, by treating the head portion of skeletal myosin subfragment-1 (S1) with the bifunctional agent dibromobimane, we introduced an intramolecular covalent cross-link which resulted in the stabilisation of an internal loop in the heavy chain structure of the head [Mornet et al. (1984) Proc. Natl Acad. Sci. USA 82, 1658-1662]. ... More
Biotinylated granulocyte/macrophage colony-stimulating factor analogues: effect of linkage chemistry on activity and binding.
Authors:Angelotti TP, Clarke MF, Longino MA, Emerson SG
Journal:Bioconjug Chem
PubMed ID:1839606
'Biotinylated granulocyte/macrophage colony-stimulating factor (GM-CSF) analogues with different linkage chemistries and levels of conjugated biotin were synthesized by reacting recombinant human GM-CSF with sulfosuccinimidyl 6-biotinamidohexanoate or biotin hydrazide/1-[3-(dimethylamino)-propyl]-3-ethylcarbodiimide. These chemically reactive forms of biotin produced derivatives biotinylated at amine or carboxyl groups, respectively. Amine-derivatized analogues of 1.2 and 3.8 mol ... More
Zero-length crosslinking between subunits delta and I of the H(+)-translocating ATPase of chloroplasts.
Authors:Beckers G, Berzborn RJ, Strotmann H
Journal:Biochim Biophys Acta
PubMed ID:1385976
'Treatment of spinach thylakoids with 1-ethyl-3-(dimethylaminopropyl)-carbodiimide (EDC)/N-hydroxysulfosuccinimide (sulfo-NHS) induced formation of a zero-length crosslink of an apparent molecular mass of 38 kDa. This product was shown, by immunodetection, to consist of subunit delta of CF1 and subunit I of CF0. The crosslink was isolated by preparative SDS gel electrophoresis and ... More
Carbodiimide as a tissue fixative in histamine immunohistochemistry and its application in developmental neurobiology.
Authors:Panula P, Häppölä O, Airaksinen MS, Auvinen S, Virkamäki A
Journal:J Histochem Cytochem
PubMed ID:3343510
'The object of this study was to develop an immunohistochemical method that could be used to study neuronal histamine, especially in nerve fibers and terminals where most previous methods have not been applicable. Three new antisera were produced in rabbits against conjugated histamine, and the fixative used in conjugation, 1-ethyl-3(3-diamethylaminopropyl)-carbodiimide ... More