Phalloidin Labeling Probes
Phalloidin Labeling Probes
Invitrogen™

Phalloidin Labeling Probes

Achieve precise and reliable F-actin staining with fluorescent and biotinylated phalloidins. Phalloidin conjugates are widely used in imaging applications to selectively label F-actin in a variety of sample types including fixed and permeabilized cells, tissue sections, and cell-free experiments.
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Catalog NumberColorExcitation Wavelength RangeDye Type
A30107Far-red650/668 nmAlexa Fluor Plus 647
A22281Blue346/442 nmAlexa Fluor™ 350
A30104Violet405/450 nmAlexa Fluor™ Plus 405
A12379Green495/518 nmAlexa Fluor™ 488
O7466Green496/520 nmOregon Green™ 488
F432Green496/516 nmFITC (Fluorescein)
A22282Yellow531/554 nmAlexa Fluor™ 532
R415Red-orange540/565 nmTRITC
A22283Orange556/570 nmAlexa Fluor™ 546
A34055Orange555/565 nmAlexa Fluor™ 555
A30106Orange555/565 nmAlexa Fluor Plus 555
B3475Red558/569 nmBODIPY™
A12380Orange-red578/600 nmAlexa Fluor™ 568
A12381Red581/609 nmAlexa Fluor™ 594
T7471Red591/608 nmTexas Red™
A22284Far-red632/647 nmAlexa Fluor™ 633
A34054Far-red633/647 nmAlexa Fluor™ 635
A22287Far-red650/668 nmAlexa Fluor™ 647
A22285Near-infrared663/690 nmAlexa Fluor™ 660
A22286Near-infrared679/702 nmAlexa Fluor™ 680
A30105Near-infrared758/784 nmAlexa Fluor™ Plus 750
B7474NoneNoneBiotin-XX
P3457NoneNonePhalloidin (unlabeled)
Catalog number A30107
Price (USD)
690.65
Online Exclusive
712.00
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Color:
Far-red
Excitation Wavelength Range:
650/668 nm
Dye Type:
Alexa Fluor Plus 647
Recurring order eligible. Learn more »
Price (USD)
690.65
Online Exclusive
712.00
Save 21.35 (3%)
Each
Add to cart
Ask our AI about this Product
Fluorescent and biotinylated phalloidins are water soluble and bind to filamentous actin (F-actin) with nanomolar affinity, making them convenient probes for labeling, identifying, and quantifying F-actin in cryopreserved tissue sections, fixed and permeabilized cells, and cell-free experiments. Phalloidin conjugates bind similarly to actin from various species, including plants and animals, enabling staining of the cytoskeleton in a wide range of samples.

A variety of phalloidin conjugates for filamentous (F-actin) staining are available, including fluorescent Alexa Fluor and Alexa Fluor Plus phalloidins, along with phalloidins conjugated to classic fluorescent dyes such as BODIPY, fluorescein, and rhodamine. Phalloidin staining is spectrally compatible with other fluorescent stains used in cellular analyses such as GFP/RFP, Qdot nanocrystals, and other Alexa Fluor conjugates and antibodies. Biotin‐XX Phalloidin can be used to visualize actin filaments via fluorescent streptavidin tags or standard enzyme-mediated avidin/streptavidin techniques such as in electron microscopy. Unlabeled phalloidin is available for use as a control in blocking F‐actin staining or in promoting polymerization.

Phalloidin conjugates bind to both large and small actin filaments with similar affinity in a 1:1 stoichiometry between phallotoxin and actin subunits. They do not bind G-actin monomers.

Alexa Fluor and Alexa Fluor Plus phalloidin conjugates for F-actin staining

Fluorescent Alexa Fluor dye conjugates of phalloidin are popular F-actin stains, offering color choices across the full spectral range. These phalloidin conjugates provide researchers with fluorescent probes that are superior in brightness and photostability compared to other spectrally similar conjugates.

Alexa Fluor Plus Phalloidin conjugates retain the same specificity for actin but offer 3-5 times greater sensitivity and brightness compared to the corresponding Alexa Fluor Phalloidin conjugate. This increased brightness is beneficial for challenging F-actin imaging, such as the super‐resolution microscopy methods SIM and STORM, and for reliable staining of actin stress fibers.

Features of phalloidin probes

  • High specificity—binds selectively to F-actin, which allows for precise labeling of actin filaments in fixed cells and cryopreserved tissues
  • Strong affinity—nanomolar binding affinity for F-actin, which ensures stable and reliable actin staining
  • Extensive fluorescent conjugate options—over twenty conjugated varieties of phalloidin
  • Compatibility with fixed samples—typically used with fixed cells and tissues, making them suitable for actin staining in detailed structural studies, immunofluorescence staining, and IHC applications
  • Multiplexing capability—the wide availability of phalloidin conjugates enables their use in combination with other fluorescent probes and antibodies for multiplex imaging. Biotinylated phalloidin can be made use of in downstream streptavidin steps.
  • Quantitative analysis—can be used for quantitative analysis of F-actin distribution and density within cells, aiding in the study of cytoskeletal dynamics. The unlabeled phalloidin can be titrated as a control.
  • Ease of use—staining is straightforward and quick
  • Excellent stability—exhibit good photostability, which is essential for prolonged imaging sessions and time-lapse studies
  • Wide applicability—used for a range of applications, including studying cell morphology, motility, and the effects of drugs on the actin cytoskeleton
For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorFar-red
Dye TypeAlexa Fluor Plus 647
Excitation Wavelength Range650/668 nm
For Use With (Equipment)Fluorescence Microscope, Flow Cytometer, Confocal Microscope, Compatible Cy5 filter set
Product LineAlexa Fluor™
Quantity1 Ea.
Shipping ConditionQualified for Ambient or Wet Ice
Label TypeAlexa Fluor Dyes
Product TypePhalloidin
SubCellular LocalizationActin
Unit SizeEach
Contents & Storage
Contains 1 vial with enough material for 300 units/slides
Store at ≤-20°C after receiving. Desiccate and protect from light.
When stored as directed, product is stable for (at least 1 year.
)
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Lot #Certificate TypeDateCatalog Number(s)
3188272Certificate of AnalysisJun 29, 2025A12381
3203004Certificate of AnalysisJun 18, 2025A30107
3163213Certificate of AnalysisJun 18, 2025A22281
3158259Certificate of AnalysisJun 18, 2025A22284
3148327Certificate of AnalysisMay 28, 2025A34055
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Safety Data Sheets

Frequently asked questions (FAQs)

We do not recommend using phalloidin conjugates for staining actin in combination with traditional Click-iT or Click-iT Plus reactions since phalloidin is extremely sensitive to the presence of copper.

For staining actin in combination with traditional Click-iT or Click-iT Plus reactions, we recommend using anti-α-actin antibodies for staining actin in the cytoskeleton. You can find a list of our actin antibodies here.

Another option would be to use the Click-iT Plus Alexa Fluor Picolyl Azide Toolkit (Cat. Nos. C10641, C10642, C10643). These Click-iT Plus toolkits provide Copper and Copper protectant separately which makes it easier to titrate the copper concentration to obtain optimal labeling with minimal copper-mediated damage. You may need to optimize the click reaction with the lowest possible concentration of copper and then perform the phalloidin staining.

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

If the F-actin is depolymerized, phalloidin will not bind. Any processing steps or any treatments/compound that can promote depolymerization would impact phalloidin binding. Also, any compounds that also bind to F-actin (without depolymerization) may affect phalloidin binding.

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

No. They differ only in the dyes attached to the phalloidin. The phalloidin has the same structure in all of the products.

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

When cells and tissues are treated with solvents such as xylene or acetone (for example during deparaffinization of tissue sections), it affects the F-actin in a way that prevents phalloidins from binding. Phalloidin may be used with cryosections, which are not typically washed with organic solvents, or anti-actin antibodies may be used.

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

Citations & References (2585)

Citations & References
Abstract
Identification of the C-terminal part of Bordetella dermonecrotic toxin as a transglutaminase for rho GTPases.
Authors:Schmidt G,Goehring UM,Schirmer J,Lerm M,Aktories K
Journal:The Journal of biological chemistry
PubMed ID:10542213
The organic anion transport polypeptide 1d1 (Oatp1d1) mediates hepatocellular uptake of phalloidin and microcystin into skate liver.
Authors:Meier-Abt F,Hammann-Hänni A,Stieger B,Ballatori N,Boyer JL
Journal:Toxicology and applied pharmacology
PubMed ID:17198718
DOCK2 is a Rac activator that regulates motility and polarity during neutrophil chemotaxis.
Authors:Kunisaki Y,Nishikimi A,Tanaka Y,Takii R,Noda M,Inayoshi A,Watanabe K,Sanematsu F,Sasazuki T,Sasaki T,Fukui Y
Journal:The Journal of cell biology
PubMed ID:16943182
Neutrophils are highly motile leukocytes, and they play important roles in the innate immune response to invading pathogens. Neutrophil chemotaxis requires Rac activation, yet the Rac activators functioning downstream of chemoattractant receptors remain to be determined. We show that DOCK2, which is a mammalian homologue of Caenorhabditis elegans CED-5 and ... More
A natural ErbB4 isoform that does not activate phosphoinositide 3-kinase mediates proliferation but not survival or chemotaxis.
Authors:Kainulainen V,Sundvall M,Määttä JA,Santiestevan E,Klagsbrun M,Elenius K
Journal:The Journal of biological chemistry
PubMed ID:10722704
The p42/p44 MAP kinase pathway prevents apoptosis induced by anchorage and serum removal.
Authors:Le Gall M,Chambard JC,Breittmayer JP,Grall D,Pouysségur J,Van Obberghen-Schilling E
Journal:Molecular biology of the cell
PubMed ID:10712523
Anchorage removal like growth factor removal induces apoptosis. In the present study we have characterized signaling pathways that can prevent this cell death using a highly growth factor– and anchorage-dependent line of lung fibroblasts (CCL39). After anchorage removal from exponentially growing cells, annexin V-FITC labeling can be detected after 8 ... More
2585 total citations

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