ReadyProbes™ Reagent F-Actin Phalloidin Conjugates
ReadyProbes™ Reagent F-Actin Phalloidin Conjugates
Invitrogen™

ReadyProbes™ Reagent F-Actin Phalloidin Conjugates

Perfect for fixed cells and tissue, ReadyProbes Reagent F-actin phalloidin conjugates offer clear visualization of actin filaments, making it perfect for cell biology, neuroscience, cancer research, and more.
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Catalog NumberColorExcitation Wavelength Range
R37112Red-Orange540/565
R37110Green495/518
Catalog number R37112
Price (CLP)
376.854
Each
Add to cart
Color:
Red-Orange
Excitation Wavelength Range:
540/565
Price (CLP)
376.854
Each
Add to cart
ActinGreen 488 ReadyProbes Reagent is a selective, high-affinity F-actin probe conjugated to our bright, photostable, green-fluorescent Alexa Fluor 488 dye. ActinGreen 488 reagent is a room temperature-stable solution of Alexa Fluor 488 Phalloidin (Cat. No. A12379) packaged in a dropper bottle. ActinRed 555 ReadyProbes Reagent is a comparable F-actin stain conjugated to the red-orange fluorescent dye tetramethylrhodamine (TRITC). ActinRed 555 reagent is a room temperature-stable solution of Rhodamine Phalloidin (Cat. No. R415) packaged in a dropper bottle.

These ready-to-use solutions combines superior brightness with exceptional F-actin staining. Phalloidin is a bi-cyclic peptide, commonly used in imaging applications to selectively label F-actin. Fluorescently labeled phalloidin has several advantages over antibodies for actin labeling, including virtually identical binding properties with actin from different species of plants and animals and low non-specific binding.

Features

  • High-affinity staining of F-actin with superior specificity compared to antibody methods
  • ActinGreen 488 Excitation/Emission: (495/518 nm), detected through standard GFP and FITC filter sets
  • ActinRed 555 Excitation/Emission: (540/565 nm), detected through standard RFP and TRITC filters sets
  • Use counterstain (i.e., DAPI or NucBlue ReadyProbes reagent) as desired

ReadyProbes format advantages

  • Ready-to-use formulation—no need to dilute, weigh, or pipette
  • Just use two drops per mL of medium to stain, incubate 30 minutes, wash, then image
  • Stable at room temperature—keep handy on the benchtop

Applications

  • For fixed and permeabilized cells or tissue
  • Fluorescence microscopy (IF/IHC/ICC)
  • High content screening, high content imaging
  • Flow cytometry

Suggestions for use

  • Both ActinRed 555 and ActinGreen 488 reagents may be added directly to fixed cells in full medium or buffer solutions
  • In most cases 2 drops/mL and an incubation time of 15–30 minutes is sufficient for bright actin staining; however, optimization may be needed for some cell types, conditions, and applications. In such cases, simply add more or fewer drops until the optimal staining intensity is obtained.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorRed-Orange
DescriptionActinRed™ 555 ReadyProbes™ Reagent (Rhodamine phalloidin)
Detection MethodFluorescence
Dye TypeTRITC (Tetramethylrhodamine Isothiocyanate)
EmissionVisible
Excitation Wavelength Range540/565
For Use With (Equipment)Confocal Microscope, EVOS™, Floid™ Cell Imaging System, Fluorescence Microscope, Flow Cytometer, Floid™ Cell Imaging System
FormLiquid
Product LineActinRed, ReadyProbes
Quantity2 dropper bottle(s) kit
TechniqueFluorescence Intensity
Label TypeFluorescent Dye
Product TypePhalloidin
SubCellular LocalizationCytoskeleton
Unit SizeEach
Contents & Storage

2 x 2.5 mL dropper bottles

Store at ≤ 25°C.

Frequently asked questions (FAQs)

Can I use the ReadyProbes reagents for flow cytometry?

This is not recommended. The ReadyProbes reagents were developed for imaging applications whereas the Ready Flow reagents were optimized for flow cytometry.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Citations & References (42)

Citations & References
Abstract
Fabrication of high specificity hollow mesoporous silica nanoparticles assisted by Eudragit for targeted drug delivery.
Authors:She X, Chen L, Velleman L, Li C, Zhu H, He C, Wang T, Shigdar S, Duan W, Kong L,
Journal:
PubMed ID:25617610
'Hollow mesoporous silica nanoparticles (HMSNs) are one of the most promising carriers for effective drug delivery due to their large surface area, high volume for drug loading and excellent biocompatibility. However, the non-ionic surfactant templated HMSNs often have a broad size distribution and a defective mesoporous structure because of the ... More
Collaborative Enhancement of Endothelial Targeting of Nanocarriers by Modulating Platelet-Endothelial Cell Adhesion Molecule-1/CD31 Epitope Engagement.
Authors:Chacko AM, Han J, Greineder CF, Zern BJ, Mikitsh JL, Nayak M, Menon D, Johnston IH, Poncz M, Eckmann DM, Davies PF, Muzykantov VR,
Journal:
PubMed ID:26153796
Nanocarriers (NCs) coated with antibodies (Abs) to extracellular epitopes of the transmembrane glycoprotein PECAM (platelet endothelial cell adhesion molecule-1/CD31) enable targeted drug delivery to vascular endothelial cells. Recent studies revealed that paired Abs directed to adjacent, yet distinct epitopes of PECAM stimulate each other's binding to endothelial cells in vitro ... More
Electrochemical behavior of bioactive coatings on cp-Ti surface for dental application.
Authors:Marques ID, Barão VA, da Cruz NC, Yuan JC, Mesquita MF, Ricomini-Filho AP, Sukotjo C, Mathew MT,
Journal:
PubMed ID:26834277
The surface characteristics and electrochemical properties of bioactive coatings produced by plasma electrolytic oxidation (PEO) with calcium, phosphorous, silicon and silver on commercially pure titanium were evaluated. PEO treatment produced a porous oxide layer, which improved the surface topography, and enriched the surface chemistry with bioactive elements, responsible for mimicking ... More
In situ measurement of magnetization relaxation of internalized nanoparticles in live cells.
Authors:Soukup D, Moise S, Céspedes E, Dobson J, Telling ND,
Journal:
PubMed ID:25562356
Magnetization relaxation mechanisms strongly influence how magnetic nanoparticles respond to high-frequency fields in applications such as magnetic hyperthermia. The dominant mechanism depends on the mobility of the particles, which will be affected in turn by their microenvironment. In this study AC susceptometry was used to follow the in situ magnetic ... More
Controlled electromechanical cell stimulation on-a-chip.
Authors:Pavesi A, Adriani G, Rasponi M, Zervantonakis IK, Fiore GB, Kamm RD,
Journal:
PubMed ID:26135970
Stem cell research has yielded promising advances in regenerative medicine, but standard assays generally lack the ability to combine different cell stimulations with rapid sample processing and precise fluid control. In this work, we describe the design and fabrication of a micro-scale cell stimulator capable of simultaneously providing mechanical, electrical, ... More