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MilliporeSigma

76245

Atto 655 NHS ester

BioReagent, suitable for fluorescence

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About This Item

UNSPSC Code:
12352108
PubChem Substance ID:
93577785
NACRES:
NA.32
MDL number:
MFCD03456137

Key Documents

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Product Name

Atto 655 NHS ester, BioReagent, suitable for fluorescence

SMILES string

[S](=O)(=O)([O-])CC1CC([N+](=C3C1=CC4=Nc5c(cc6c(c5)CCCN6CC)OC4=C3)CCCC(=O)ON2C(=O)CCC2=O)(C)C

InChI

1S/C31H36N4O8S/c1-4-33-11-5-7-19-13-22-26(15-24(19)33)42-27-16-25-21(14-23(27)32-22)20(18-44(39,40)41)17-31(2,3)34(25)12-6-8-30(38)43-35-28(36)9-10-29(35)37/h13-16,20H,4-12,17-18H2,1-3H3

InChI key

SPDKWNQUMMQOKX-UHFFFAOYSA-N

product line

BioReagent

assay

≥90.0% (HPLC)

form

powder

manufacturer/tradename

ATTO-TEC GmbH

extent of labeling

≥90.0%

λ

in ethanol (with 0.1% trifluoroacetic acid)

UV absorption

λ: 650.0-656.0 nm Amax

suitability

suitable for coupling to amines
suitable for fluorescence

storage temp.

−20°C

Quality Level

100

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This Item
759991698661909
Sigma-Aldrich

Sigma-Aldrich

76245

Atto 655 NHS ester

Sigma-Aldrich

Sigma-Aldrich

75999

Atto 680 NHS ester

Sigma-Aldrich

Sigma-Aldrich

16986

Atto 700 NHS-ester

Sigma-Aldrich

Sigma-Aldrich

61909

Atto Rho14 NHS ester

suitability

suitable for coupling to amines, suitable for fluorescence

suitability

-

suitability

-

suitability

-

form

powder

form

powder

form

powder

form

solid

assay

≥90.0% (HPLC)

assay

≥90% (HPLC), ≥90% (coupling of degree)

assay

≥90% (coupling to amine, HPLC)

assay

≥90.0% (HPLC)

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

product line

BioReagent

product line

BioReagent

product line

BioReagent

product line

BioReagent

Application

Atto fluorescent labels are designed for high sensitivity applications, including single molecule detection. Atto labels have rigid structures that do not show any cis-trans-isomerization. Thus these labels display exceptional intensity with minimal spectral shift on conjugation.

Legal Information

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

Storage Class

11 - 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
BCCP2436
BCCN4653
BCCM6568
BCCM7763
BCCL7621

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Gerald Giller et al.
Nucleic acids research, 31(10), 2630-2635 (2003-05-09)
Fluorescent-labeled DNA is generated through enzymatic incorporation of fluorophore-linked 2'-deoxyribonucleoside-5'-triphosphates (dNTPs) by DNA polymerases. We describe the synthesis of a variety of dye-labeled dNTPs. Amino-linker-modified 5'-triphosphates of all four naturally occurring nucleobases were used as precursors. Commercially available dyes were
Taurai Tasara et al.
Nucleic acids research, 31(10), 2636-2646 (2003-05-09)
The modification of nucleic acids using nucleotides linked to detectable reporter or functional groups is an important experimental tool in modern molecular biology. This enhances DNA or RNA detection as well as expanding the catalytic repertoire of nucleic acids. Here
Highly sensitive protease assay using fluorescence quenching of peptide probes based on photoinduced electron transfer.
Nicole Marmé et al.
Angewandte Chemie (International ed. in English), 43(29), 3798-3801 (2004-07-20)
Ye Chen et al.
Biomedical optics express, 10(3), 1257-1272 (2019-03-21)
Open-top light-sheet microscopy is a technique that can potentially enable rapid ex vivo inspection of large tissue surfaces and volumes. Here, we have optimized an open-top light-sheet (OTLS) microscope and image-processing workflow for the comprehensive examination of surgical margin surfaces
Nicole Marmé et al.
Bioconjugate chemistry, 14(6), 1133-1139 (2003-11-20)
Steady-state and time-resolved fluorescence measurements were performed to elucidate the fluorescence quenching of oxazine, rhodamine, carbocyanine, and bora-diaza-indacene dyes by amino acids. Among the natural amino acids, tryptophan exhibits the most pronounced quenching efficiency. Especially, the red-absorbing dyes ATTO 655
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