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.
製品番号(カタログ番号)励起波長域染色剤タイプ
P3457NoneNonePhalloidin (unlabeled)
A22281Blue346⁄442Alexa Fluor™ 350
A30104Violet405/450Alexa Fluor™ Plus 405
A12379Green495⁄518Alexa Fluor™ 488
O7466Green496⁄520Oregon Green™ 488
F432Green496⁄516FITC(フルオレセイン)
A22282Yellow531⁄554Alexa Fluor™ 532
R415Red-orange540⁄565TRITC(テトラメチルローダミンイソチオシアン酸塩)
A22283Orange556⁄570Alexa Fluor™ 546
A34055Orange555⁄565Alexa Fluor™ 555
A30106Orange555/565 nmAlexa Fluor Plus 555
B3475Red558⁄569BODIPY™
A12380Orange-red578⁄600Alexa Fluor™ 568
A12381Red581⁄609Alexa Fluor™ 594
T7471Red591⁄608Texas Red™
A22284Far-red632⁄647Alexa Fluor™ 633
A34054Far-red633⁄647Alexa Fluor™ 635
A22287Far-red650⁄668Alexa Fluor™ 647
A30107Far-red650/668 nmAlexa Fluor Plus 647
A22285Near-infrared663⁄690Alexa Fluor™ 660
A22286Near-infrared679⁄702Alexa Fluor™ 680
A30105Near-infrared758/784Alexa Fluor™ Plus 750
B7474NoneNoneビオチン-XX
製品番号(カタログ番号) P3457
価格(JPY)
64,600
Each
お問い合わせください ›
色:
None
励起波長域:
None
染色剤タイプ:
Phalloidin (unlabeled)
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
研究用にのみ使用できます。診断用には使用いただけません。
仕様
None
染色剤タイプPhalloidin (unlabeled)
励起波長域None
使用対象 (装置)Fluorescence Microscope, Flow Cytometer, Confocal Microscope
数量1 mg
出荷条件室温
標識タイプ非標識
製品タイプファロイジン
SubCellular Localizationアクチン、細胞骨格, Cytoskeleton
Unit SizeEach
組成および保存条件
フリーザー(-5℃~-30℃)に保存。

よくあるご質問(FAQ)

Can I combine Click-iT or Click-iT Plus reactions with phalloidin conjugates used for actin staining?

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.

引用および参考文献 (111)

引用および参考文献
Abstract
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
Mutational analysis of the role of hydrophobic residues in the 338-348 helix on actin in actomyosin interactions.
Authors:Miller CJ, Doyle TC, Bobkova E, Botstein D, Reisler E
Journal:Biochemistry
PubMed ID:8619986
Yeast actin mutants with alanines replacing I341 and I345 were studied to assess the role of hydrophobic residues in the alpha-helix 338-348 in interactions with myosin. In structural models of the actomyosin complex, this helix on actin was assigned a prominent role in the strong binding of myosin to actin. ... More
Myosin is involved in postmitotic cell spreading.
Authors:Cramer LP, Mitchison TJ
Journal:J Cell Biol
PubMed ID:7559774
'We have investigated a role for myosin in postmitotic Potoroo tridactylis kidney (PtK2) cell spreading by inhibitor studies, time-lapse video microscopy, and immunofluorescence. We have also determined the spatial organization and polarity of actin filaments in postmitotic spreading cells. We show that butanedione monoxime (BDM), a known inhibitor of muscle ... More
The sequence of the myosin 50-20K loop affects Myosin's affinity for actin throughout the actin-myosin ATPase cycle and its maximum ATPase activity.
Authors:Murphy CT, Spudich JA
Journal:Biochemistry
PubMed ID:10090768
'We are interested in the role that solvent-exposed, proteolytically sensitive surface loops play in myosin function. The 25-50K loop, or loop 1, is near the ATP binding site, while the 50-20K loop (loop 2) is in the actin binding site. Through chimeric studies, we have found that loop 1 affects ... More
Gelsolin displaces phalloidin from actin filaments. A new fluorescence method shows that both Ca2+ and Mg2+ affect the rate at which gelsolin severs F-actin.
Authors:Allen PG, Janmey PA
Journal:J Biol Chem
PubMed ID:7806519
'We describe an assay for measuring both the extent and kinetics of the severing of F-actin, based on the enhanced fluorescence emission of tetramethylrhodamine-phalloidin bound to F-actin. The enhanced fluorescence is lost after exposure to active gelsolin by displacement of the phalloidin from actin during severing. This assay requires small ... More