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Sigma-Aldrich

Abberior® STAR 488, NHS ester

for STED application

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About This Item

UNSPSC Code:
12352200
NACRES:
NA.32

form

solid

concentration

≥50.0% (degree of coupling)

solubility

DMF: 1 mg/mL, clear

fluorescence

λex 510 nm; λem 514-534 nm in PBS, pH 7.4

storage temp.

−20°C

General description

Abberior STAR 488 is the latest development for STED microscopy. It is a very bright green fluorescent dye that can be very effectively excited at the prominent 488 nm laser line. Abberior STAR 488 can substitute dyes like Oregon Green 488, Atto 488 or Alexa Fluor 488.
STED: The dye can most effectively be depleted in STED microscopy at 585-605 nm.

Abberior STAR 488 is the dye of choice for excitation at 488 nm. Even more, the dye is particularly signed and tested for 2-color STED microscopy in combination with our STAR 440SX rusing a 590nm laser. The dye has been very successfully tested in the Leica 2-color TCS STED CW microscope.

Key Features
  • STED dye of choice at 488 nm excitation
  • Ideal depletion behavior in STED microscopy ~590 nm
  • 2-color labeling partner with STAR 440SX for 2-color STED microscopy

Absorption Maximum, λmax: 503 nm (PBS, pH 7.4)
Extinction Coefficient, ε(λmax): 65′000 M-1cm-1 (PBS, pH 7.4)
Correction Factor, CF260 = ε260/εmax: 0.28 (PBS, pH 7.4)
Correction Factor, CF280 = ε280/εmax: 0.14 (PBS, pH 7.4)
Fluorescence Maximum, λfl: 524nm (PBS, pH 7.4)
Recommended STED Wavelength, λSTED: 585 - 605 nm
Fluorescence Quantum Yield, η: 0.89 (PBS, pH 7.4)
Fluorescence Lifetime, τ: 3.9 ns (MeOH)

Application

Anti-Rabbit IgG-Abberior® STAR 488 antibody has been used as a secondary antibody:
  • for fluorescent immunohistochemistry in prostate cancer cell lines, PPC-1 and TSU-Pr1
  • for immunofluorescence in HeLa and monkey kidney COS-7 cells
  • for STED (stimulated emission depletion) microscopy in OLN-t40-α-syn cells (oligodendroglial cells)

Suitability

Designed and tested for fluorescent super-resolution microscopy

Legal Information

Atto is a trademark of Atto-Tec GmbH
abberior is a registered trademark of Abberior GmbH

related product

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Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Katharina Pukaß et al.
Frontiers in cellular neuroscience, 9, 163-163 (2015-05-23)
α-Synuclein (α-syn) positive glial cytoplasmic inclusions (GCI) originating in oligodendrocytes (ODC) are a characteristic hallmark in multiple system atrophy (MSA). Their occurrence may be linked to a failure of the ubiquitin proteasome system (UPS) or the autophagic pathway. For proteasomal
Combination of axitinib and dasatinib for anti-cancer activities in two prostate cancer cell lines.
Peng N
Bangladesh Journal of Pharmacology, 11, 10-10 (2016)
Giuseppe Vicidomini et al.
Methods (San Diego, Calif.), 66(2), 124-130 (2013-07-03)
Stimulation emission depletion (STED) microscopy breaks the spatial resolution limit of conventional light microscopy while retaining its major advantages, such as working under physiological conditions. These properties make STED microscopy a perfect tool for investigating dynamic sub-cellular processes in living
Marcus Dyba et al.
Nature biotechnology, 21(11), 1303-1304 (2003-10-21)
We report immunofluorescence imaging with a spatial resolution well beyond the diffraction limit. An axial resolution of approximately 50 nm, corresponding to 1/16 of the irradiation wavelength of 793 nm, is achieved by stimulated emission depletion through opposing lenses. We
T A Klar et al.
Optics letters, 24(14), 954-956 (2007-12-13)
We overcame the resolution limit of scanning far-field fluorescence microscopy by disabling the fluorescence from the outer part of the focal spot. Whereas a near-UV pulse generates a diffraction-limited distribution of excited molecules, a spatially offset pulse quenches the excited

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