Phalloidin-Janelia Fluor® 646

Catalog # Availability Size / Price Qty
7201/12U
Phalloidin-Janelia Fluor® 646 | Janelia Fluor Dyes
3 Images
Description: Red-fluorescent F-actin probe. Binds and labels F-actin. Used for: F-actin labelling. Application: confocal microscopy, super resolution microscopy (SRM) including dSTORM & STED, flow cytometry
Alternative Names: Phalloidin-JF646

Purity: ≥90%

Product Details
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Biological Activity

Key information: Phalloidin-Janelia Fluor® 646 is a red fluorescent F-actin probe. It binds and labels specifically F-actin.

Used for: Phalloidin-Janelia Fluor® 646 can be used to visualize and quantify F-actin in tissue sections, cell cultures or cell-free experiments with optimal results in formaldehyde-fixed and permeabilized cells.

Application: confocal microscopy, super-resolution microscopy (SRM) including dSTORM and STED and flow cytometry.

Properties and Photophysical Data: Phalloidin-Janelia Fluor® 646 is composed of the F-actin probe, Phalloidin (Cat. No. 4535), conjugated to Janelia Fluor® 646 (Cat. No. 6148). Excitation and emission maxima (λ) are 646 nm and 664 nm, respectively; quantum yield = 0.54; extinction coefficient = 152,000 M-1cm-1.

Scientific Data

Confocal Microscopy Application of Phalloidin-Janelia Fluor® 646 View Larger

Application of Phalloidin-Janelia Fluor® 646. HeLa cells were fixed for 10 minutes with 4% formaldehyde in PBS and permeabilized with PBS/0.25% Triton X-100 for 6 minutes. An additional post-fixation step was performed twice with 1% formaldehyde in PBS followed by 3 washes with PBS. Phalloidin Janelia Fluor® 646 was prepared as a 10 μM stock solution diluted in methanol and diluted to a working concentration of 20 nM in PBS. Stained cells were imaged with a Leica SP8X WLL upright confocal microscope. Image kindly provided by Brigitte Bergner, Steffen Dietzel, Core Facility Bioimaging at the Biomedical Center of the Ludwig-Maximilians-Universität München.

Confocal Microscopy Application of Phalloidin-Janelia Fluor® 646 View Larger

Application of Phalloidin-Janelia Fluor® 646. HeLa cells were fixed for 10 minutes with 4% formaldehyde in PBS and permeabilized with PBS/0.25% Triton X-100 for 6 minutes. An additional post-fixation step was performed twice with 1% formaldehyde in PBS followed by 3 washes with PBS. Phalloidin Janelia Fluor® 646 was prepared as a 10 μM stock solution diluted in methanol and diluted to a working concentration of 20 nM in PBS. Stained cells were imaged with a Leica SP8X WLL upright confocal microscope. Image kindly provided by Brigitte Bergner, Steffen Dietzel, Core Facility Bioimaging at the Biomedical Center of the Ludwig-Maximilians-Universität München.

Optical Data for Phalloidin-Janelia Fluor® 646

Phalloidin-Janelia Fluor<sup>®</sup> 646 Dye Spectra
Emission Color Red
Brightness
λabs 646 nm
λem 664 nm
Extinction Coefficient (ε) 152,000 M-1cm-1
Quantum Yield (φ) 0.54
Closest Laser line 640 nm
Application Confocal Imaging, dSTORM, STED, Flow Cytometry

Plan Your Experiments

Use our spectra viewer to interactively plan your experiments, assessing multiplexing options. View the excitation and emission spectra for our fluorescent dye range and other commonly used dyes.

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Technical Data

M.Wt:
1266.51
Formula:
C64H75N11O13SSi
Purity:
≥90%
Storage:
Store at -20°C

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Additional Information

Licensing Caveats:
Sold under license from the Howard Hughes Medical Institute, Janelia Research Campus

Background References

  1. Effects of cytochalasin and phalloidin on actin.
    Cooper
    J.Cell Biol., 1987;105:1473
  2. A general method to improve fluorophores for live-cell and single-molecule microscopy.
    Grimm et al.
    Nat.Methods, 2015;12:244

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