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Key Documents

41986

Sigma-Aldrich

Atto 550 azide

BioReagent, suitable for fluorescence

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About This Item

UNSPSC Code:
12352125
NACRES:
NA.32

product line

BioReagent

Quality Level

assay

>90% (HPLC)

manufacturer/tradename

ATTO-TEC GmbH

transmittance

254 nm
550 nm

fluorescence

λex 554 nm; λem 576 nm±10 nm in 0.1 M phosphate pH 7.0

λ

(ethanol with 0.1% trifluoroacetic acid)

UV absorption

λ: 553-559 nm Amax

suitability

suitable for fluorescence

storage temp.

−20°C

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Smart-aggregation imaging for single molecule localization with SPAD cameras.
Gyongy, I.; et al.
arXiv (2016)
Robert H Meltzer et al.
Lab on a chip, 11(5), 863-873 (2011-01-21)
Rapid, specific, and sensitive detection of airborne bacteria, viruses, and toxins is critical for biodefense, yet the diverse nature of the threats poses a challenge for integrated surveillance, as each class of pathogens typically requires different detection strategies. Here, we
A molecular toolkit for population genetic investigations of the ash dieback pathogen Hymenoscyphus pseudoalbidus.
Gross, A., et al.
Forest Pathology, 42, 252-264 (2012)
Rahul Roy et al.
Nature methods, 5(6), 507-516 (2008-05-31)
Single-molecule fluorescence resonance energy transfer (smFRET) is one of the most general and adaptable single-molecule techniques. Despite the explosive growth in the application of smFRET to answer biological questions in the last decade, the technique has been practiced mostly by
Eric J White et al.
Clinical chemistry, 55(12), 2121-2129 (2009-10-10)
Epidemiologic studies require identification or typing of microbial strains. Macrorestriction DNA mapping analyzed by pulsed-field gel electrophoresis (PFGE) is considered the current gold standard of genomic typing. This technique, however, is difficult to implement because it is labor-intensive and difficult

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