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Merck
CN

93259

Atto 610-NHS ester

BioReagent, suitable for fluorescence, ≥90% (HPLC)

Synonym(s):

Atto 610 N-succinimidyl ester

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About This Item

Empirical Formula (Hill Notation):
C29H34ClN3O8
Molecular Weight:
588.05
NACRES:
NA.32
PubChem Substance ID:
57653526
UNSPSC Code:
12352200
MDL number:
MFCD03456135

Key Documents

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Product Name

Atto 610-NHS ester, BioReagent, suitable for fluorescence, ≥90% (HPLC)

InChI

1S/C29H34N3O4.ClHO4/c1-29(2)23-17-22(30(3)4)10-9-19(23)15-21-16-20-7-5-13-31(25(20)18-24(21)29)14-6-8-28(35)36-32-26(33)11-12-27(32)34;2-1(3,4)5/h9-10,15-18H,5-8,11-14H2,1-4H3;(H,2,3,4,5)/q+1;/p-1

SMILES string

[O-]Cl(=O)(=O)=O.C\[N+](C)=C1/C=CC2=Cc3cc4CCCN(CCCC(=O)ON5C(=O)CCC5=O)c4cc3C(C)(C)C2=C1

InChI key

LTARFUQRQOKXLA-UHFFFAOYSA-M

product line

BioReagent

assay

≥90% (HPLC)
≥90% (degree of coupling)

form

powder

manufacturer/tradename

ATTO-TEC GmbH

λ

in ethanol (with 0.1% trifluoroacetic acid)

UV absorption

λ: 613-619 nm Amax

suitability

suitable for fluorescence

detection method

fluorometric

storage temp.

−20°C

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Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ9360
BCCJ3537
BCCJ1292
BCCH8447
BCCG5661

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Serpins regulate serine proteases by forming metastable covalent complexes with their targets. The protease docks with the serpin and cleaves the serpin's reactive center loop (RCL) forming an acylenzyme intermediate. Cleavage triggers insertion of the RCL into beta sheet A
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Over the last years, there has been an explosion in the number of developments and applications of CE and microchip-CE. In part, this growth has been the direct consequence of recent developments in instrumentation associated with CE. This review, which
A membrane-bound antiparallel dimer of rat islet amyloid polypeptide.
Abhinav Nath et al.
Angewandte Chemie (International ed. in English), 50(46), 10859-10862 (2011-09-29)
Lu Liu et al.
Protein science : a publication of the Protein Society, 16(11), 2403-2411 (2007-10-27)
Serpins inhibit serine proteases by mechanically disrupting the protease active site. The protease first reacts with the serpin's reactive center loop (RCL) to form an acylenzyme. Then the RCL inserts into a beta-sheet in the body of the serpin, translocating
Xiao X Han et al.
Analytical chemistry, 80(17), 6567-6572 (2008-07-30)
A simple and effective protocol for detections of protein-protein and protein-small molecule interactions has been developed. After interactions between proteins and their corresponding ligands, we employed colloidal silver staining for producing active substrates for surface-enhanced Raman scattering (SERS) and surface-enhanced
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