![7-Diethylamino-3-[N-(2-maleimidoethyl)carbamoyl]coumarin BioReagent, suitable for fluorescence, ≥97.0% (HPLC)](/deepweb/assets/sigmaaldrich/product/structures/341/038/a7e0c464-8abe-4eb0-b253-6537f649d89c/640/a7e0c464-8abe-4eb0-b253-6537f649d89c.png)
The product specification requires an emission wavelength range of 460-470nm. The product is not screened for excitation wavelength, however it is expected to fall within a range of 416 to 425 nm. The compound is typically used for real-time measurements for the release of inorganic phosphates during enzymatic reaction when MDCC is conjugated to a mutant phosphate-binding protein . Please see the link below to review a publication that may be of interest:
https://pubs.acs.org/doi/10.1021/bi9804277
05019
7-Diethylamino-3-[N-(2-maleimidethyl)carbamoyl]cumarin
BioReagent, suitable for fluorescence, ≥97.0% (HPLC)
Synonym(e):
MDCC
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Über diesen Artikel
Empirische Formel (Hill-System):
C20H21N3O5
CAS-Nummer:
Molekulargewicht:
383.40
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.32
MDL number:
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Unterstützung erhaltenInChI key
IXQPRUQVJIJUEB-UHFFFAOYSA-N
InChI
1S/C20H21N3O5/c1-3-22(4-2)14-6-5-13-11-15(20(27)28-16(13)12-14)19(26)21-9-10-23-17(24)7-8-18(23)25/h5-8,11-12H,3-4,9-10H2,1-2H3,(H,21,26)
product line
BioReagent
assay
≥97.0% (HPLC)
suitability
suitable for fluorescence
Quality Level
1 of 4
Dieser Artikel | G7627 | M9307 | HPA074550 |
|---|---|---|---|
| suitability suitable for fluorescence | suitability - | suitability - | suitability - |
| Quality Level 100 | Quality Level 200 | Quality Level 200 | Quality Level - |
| assay ≥97.0% (HPLC) | assay ≥90% | assay - | assay - |
| product line BioReagent | product line - | product line - | product line Prestige Antibodies® Powered by Atlas Antibodies |
Application
Thiol-reaktive Sonde für Protein-Markierung[1]
7-Diethylamino-3-[N-(2-maleimidoethyl)carbamoyl]coumarin is utilized as a fluoresencent biological sensing device . Used for real-time measurements for the release of inorganic phosphates during enzymatic reaction when MDCC is conjugated to a mutant phosphate-binding protein . Also, utilized for intramolecular fluorescence energy transfer (FRET) experiments .
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A Vandecandelaere et al.
Biochemistry, 38(25), 8179-8188 (1999-07-01)
The molecular mechanism underlying microtubule dynamic instability depends on the relationship between the addition of tubulin-GTP to a growing microtubule and its hydrolysis in the microtubule lattice to tubulin-GDP, with release of inorganic phosphate (Pi). Since this relationship remains controversial
Z H He et al.
The Journal of physiology, 501 ( Pt 1), 125-148 (1997-05-15)
1. The rate of appearance of inorganic phosphate (Pi) and hence the ATPase activity of rabbit psoas muscle in single permeabilized muscle fibres initially in rigor was measured following laser flash photolysis of the P3-1-(2-nitrophenyl)ethyl ester of ATP (NPE-caged ATP)
Jeremiah W Hanes et al.
Chemical communications (Cambridge, England), 47(8), 2273-2275 (2010-12-03)
This communication describes the development of a thiamin sensor based on the bacterial thiamin binding protein. A triple mutant (C48S, C50S, S62C) of TbpA was labeled on C62 with N-[2-(L-maleimidyl)ethyl]-7-(diethylamino)coumarin-3-carboxamide (MDCC). Thiamin binding to this protein reduced the coumarin fluorescence
Yu-Chih Tsai et al.
Biochemistry, 45(32), 9675-9687 (2006-08-09)
We show that T7 DNA polymerase exists in three distinct structural states, as reported by a conformationally sensitive fluorophore attached to the recognition (fingers) domain. The conformational change induced by a correct nucleotide commits the substrate to the forward reaction
M Brune et al.
Biochemistry, 33(27), 8262-8271 (1994-07-12)
A probe has been developed that can rapidly measure micromolar concentrations of inorganic phosphate (Pi), in particular to follow the release of Pi in real time from enzymes such as phosphatases. Its application is described to investigate the mechanism of
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