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92637

Atto 565-Biotin

Synonym(s):

Biotin-Atto 565

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1 MG

¥19,530

¥19,530

List Price¥27,900Save 30%

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About This Item

Empirical Formula (Hill Notation):
C46H57ClN6O10S
Molecular Weight:
921.50
MDL number:
UNSPSC Code:
12352108
NACRES:
NA.32

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Assay

90% (HPLC)

Quality Level

manufacturer/tradename

ATTO-TEC GmbH

fluorescence

λex 565 nm; λem 590 nm in 0.1 M phosphate pH 7.0

λ

in ethanol (with 0.1% trifluoroacetic acid)

storage temp.

−20°C

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This Item
432089360628616
fluorescence

λex 565 nm; λem 590 nm in 0.1 M phosphate pH 7.0

fluorescence

-

fluorescence

-

fluorescence

λex 437 nm; λem 483 nm in 0.1 M phosphate pH 7.0

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

assay

90% (HPLC)

assay

≥90.0% (HPLC)

assay

≥90.0% (HPLC)

assay

≥95.0% (HPCE)

manufacturer/tradename

ATTO-TEC GmbH

manufacturer/tradename

ATTO-TEC GmbH

manufacturer/tradename

ATTO-TEC GmbH

manufacturer/tradename

ATTO-TEC GmbH

λ

in ethanol (with 0.1% trifluoroacetic acid)

λ

in ethanol (with 0.1% trifluoroacetic acid)

λ

in ethanol (with 0.1% trifluoroacetic acid)

λ

-

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

92637-1MG-BULK-F:
92637-VAR-F:
92637-BULK-F:
92637-1MG-F:


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Ashwanth C Francis et al.
Cell host & microbe, 23(4), 536-548 (2018-04-13)
The HIV-1 core consists of capsid proteins (CA) surrounding viral genomic RNA. After virus-cell fusion, the core enters the cytoplasm and the capsid shell is lost through uncoating. CA loss precedes nuclear import and HIV integration into the host genome
Suman Lata et al.
Journal of the American Chemical Society, 128(7), 2365-2372 (2006-02-16)
Labeling of proteins with fluorescent dyes offers powerful means for monitoring protein interactions in vitro and in live cells. Only a few techniques for noncovalent fluorescence labeling with well-defined localization of the attached dye are currently available. Here, we present
Łukasz Krzemiński et al.
Journal of the American Chemical Society, 133(38), 15085-15093 (2011-08-26)
A combined fluorescence and electrochemical method is described that is used to simultaneously monitor the type-1 copper oxidation state and the nitrite turnover rate of a nitrite reductase (NiR) from Alcaligenes faecalis S-6. The catalytic activity of NiR is measured
Takao Nakata et al.
The Journal of cell biology, 194(2), 245-255 (2011-07-20)
Polarized transport in neurons is fundamental for the formation of neuronal circuitry. A motor domain-containing truncated KIF5 (a kinesin-1) recognizes axonal microtubules, which are enriched in EB1 binding sites, and selectively accumulates at the tips of axons. However, it remains
Marie-Luise Humpert et al.
Proteomics, 12(12), 1938-1948 (2012-05-25)
PTMs of extracellular domains of membrane proteins can influence antibody binding and give rise to ambivalent results. Best proof of protein expression is the use of complementary methods to provide unequivocal evidence. CXCR7, a member of the atypical chemokine receptor

Articles

Atto dyes are a series of fluorescent dyes that meet the critical needs of modern fluorescent technologies.

Questions

  1. How to dissolve Atto 565-Biotin, considering I want the dye to permeate cells in culture?

    1 answer
    1. The data sheet available for 92637 shows the spectrum. There is a note on the spectrum that states "in aqueous solution". Information from the supplier confirms that the product is soluble in water. The dye is also soluble in ethanol with 0.1% trifluoroacetic acid. No maximum solubility data is available. The end user should determine the working concentration.

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