Phalloidin Conjugates

iFluor® 532

This orange fluorescent phalloidin conjugate (equivalent to Alexa Fluor® 532-labeled phalloidin) selectively binds to F-actins. Used at nanomolar concentrations, phalloidin derivatives are convenient probes for labeling, identifying and quantitating F-actins in formaldehyde-fixed and permeabilized tissue sections, cell cultures or cell-free experiments. Phalloidin binds to actin filaments much more tightly than to actin monomers, leading to a decrease in the rate constant for the dissociation of actin subunits from filament ends, essentially stabilizing actin filaments through the prevention of filament depolymerization. Moreover, phalloidin is found to inhibit the ATP hydrolysis activity of F-actin. Phalloidin functions differently at various concentrations in cells. When introduced into the cytoplasm at low concentrations, phalloidin recruits the less polymerized forms of cytoplasmic actin as well as filamin into stable "islands" of aggregated actin polymers, yet it does not interfere with stress fibers, i.e. thick bundles of microfilaments. The property of phalloidin is a useful tool for investigating the distribution of F-actin in cells by labeling phalloidin with fluorescent analogs and using them to stain actin filaments for light microscopy. Fluorescent derivatives of phalloidin have turned out to be enormously useful in localizing actin filaments in living or fixed cells as well as for visualizing individual actin filaments in vitro. Fluorescent phalloidin derivatives have been used as an important tool in the study of actin networks at high resolution. AAT Bioquest offers a variety of fluorescent phalloidin derivatives with different colors for multicolor imaging applications.

Example protocol

AT A GLANCE

Protocol Summary

Prepare samples in microplate wells
Remove liquid from samples in the plate
Add Phalloidin-iFluor™ 532 Conjugate solution (100 μL/well)
Stain the cells at room temperature for 20 to 90 minutes
Wash the cells
Examine the specimen under microscope with TRITC filter

Important Warm the vial to room temperature and centrifuge briefly before opening.

Storage and Handling Conditions

The solution should be stable for at least 6 months if store at -20 °C. Protect the fluorescent conjugates from light, and avoid freeze/thaw cycles.
Note Phalloidin is toxic, although the amount of toxin present in a vial could be lethal only to a mosquito (LD50 of phalloidin = 2 mg/kg), it should be handled with care.

PREPARATION OF WORKING SOLUTION

Phalloidin-iFluor™ 532 Conjugate working solution

Add 1 µL of Phalloidin-iFluor™ 532 Conjugate solution to 1 mL of PBS with 1% BSA.
Note The stock solution of phalloidin conjugate should be aliquoted and stored at -20 °C. protected from light.
Note Different cell types might be stained differently. The concentration of phalloidin conjugate working solution should be prepared accordingly.

SAMPLE EXPERIMENTAL PROTOCOL

Stain the cells

Perform formaldehyde fixation. Incubate cells with 3.0–4.0 % formaldehyde in PBS at room temperature for 10–30 minutes.
Note Avoid any methanol containing fixatives since methanol can disrupt actin during the fixation process. The preferred fixative is methanol-free formaldehyde.
Rinse the fixed cells 2–3 times in PBS.
Optional: Add 0.1% Triton X-100 in PBS into fixed cells for 3 to 5 minutes to increase permeability. Rinse the cells 2–3 times in PBS.
Add 100 μL/well (96-well plate) of Phalloidin-iFluor™ 532 Conjugate working solution into the fixed cells, and stain the cells at room temperature for 20 to 90 minutes.
Rinse cells gently with PBS 2 to 3 times to remove excess phalloidin conjugate before plating, sealing and imaging under microscope with TRITC filter set.

Spectrum

Open in Advanced Spectrum Viewer

Alternative formats

Name	Conjugate
Phalloidin-iFluor® 488 Conjugate	iFluor 488
Phalloidin-iFluor® 647 Conjugate	iFluor 647
Phalloidin-iFluor® 594 Conjugate	iFluor 594
Phalloidin-iFluor® 555 Conjugate	iFluor 555
Phalloidin-iFluor® 633 Conjugate	iFluor 633
Phalloidin-iFluor® 532 Conjugate	iFluor 532
Phalloidin-iFluor® 405 Conjugate	iFluor 405
Phalloidin-iFluor® 514 Conjugate	iFluor 514
Phalloidin-iFluor® 350 Conjugate	iFluor 350
Phalloidin-California Red Conjugate	California Red
Phalloidin-Tetramethylrhodamine Conjugate	TRITC
Phalloidin-iFluor® 700 Conjugate	iFluor 700
Phalloidin-AMCA Conjugate	AMCA
Phalloidin-Biotin Conjugate	Biotin
Phalloidin-iFluor® 790 Conjugate	iFluor 790
XFD594 Phalloidin XFD594 Same Structure to Alexa Fluor™ 594	Alexa Fluor 594
Phalloidin-iFluor® 750 Conjugate	iFluor 750
Phalloidin-iFluor® 680 Conjugate	iFluor 680
Phalloidin-Fluorescein Conjugate	Fluorescein
XFD350 Phalloidin XFD350 Same Structure to Alexa Fluor™ 350	Alexa Fluor 350
XFD488 Phalloidin XFD488 Same Structure to Alexa Fluor™ 488	Alexa Fluor 488
XFD647 Phalloidin equivalent to Alexa Fluor® 647 phalloidin	Alexa Fluor 647
Phalloidin CAS#: 17466-45-4	Unlabeled
Phalloidin-iFluor® 660 Conjugate	iFluor 660
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Product family

Name	Excitation (nm)	Emission (nm)	Extinction coefficient (cm ^-1 M ^-1)	Quantum yield	Correction Factor (260 nm)	Correction Factor (280 nm)
Phalloidin-iFluor® 350 Conjugate	345	450	20000¹	0.95¹	0.83	0.23
Phalloidin-iFluor® 405 Conjugate	403	427	37000¹	0.91¹	0.48	0.77
Phalloidin-iFluor® 488 Conjugate	491	516	75000¹	0.9¹	0.21	0.11
Phalloidin-iFluor® 514 Conjugate	511	527	75000¹	0.83¹	0.265	0.116
Phalloidin-iFluor® 555 Conjugate	557	570	100000¹	0.64¹	0.23	0.14
Phalloidin-iFluor® 594 Conjugate	587	603	200000¹	0.53¹	0.05	0.04
Phalloidin-iFluor® 633 Conjugate	640	654	250000¹	0.29¹	0.062	0.044
Phalloidin-iFluor® 647 Conjugate	656	670	250000¹	0.25¹	0.03	0.03
Phalloidin-iFluor® 680 Conjugate	684	701	220000¹	0.23¹	0.097	0.094
Phalloidin-iFluor® 700 Conjugate	690	713	220000¹	0.23¹	0.09	0.04
Phalloidin-iFluor® 750 Conjugate	757	779	275000¹	0.12¹	0.044	0.039
Phalloidin-iFluor® 790 Conjugate	787	812	250000¹	0.13¹	0.1	0.09
Phalloidin-iFluor® 660 Conjugate	663	678	250000¹	0.26¹	0.07	0.08
iFluor® 532-streptavidin conjugate	537	560	90000¹	0.68¹	0.26	0.16
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Citations

View all 35 citations: Citation Explorer

Pesticide Efficiency of Environment-Friendly Transition Metal-Doped Magnetite Nanoparticles
Authors: Shahzadi, Shamaila and Hassan, Jalees Ul and Oneeb, Muhammad and Riaz, Saira and Sharif, Rehana and Ban, Dayan
Journal: Nanomaterials (2024): 218

Atomic force microscopy--based assessment of multimechanical cellular properties for classification of graded bladder cancer cells and cancer early diagnosis using machine learning analysis
Authors: Zhu, Xinyao and Qin, Rui and Qu, Kaige and Wang, Zuobin and Zhao, Xuexia and Xu, Wei
Journal: Acta Biomaterialia (2023): 358--373

Hypothiocyanous Acid Disrupts the Barrier Function of Brain Endothelial Cells
Authors: van Leeuwen, Eveline and Hampton, Mark B and Smyth, Leon CD
Journal: Antioxidants (2022): 608

Synthetic Collagen-like Polymer That Undergoes a Sol--Gel Transition Triggered by O--N Acyl Migration at Physiological pH
Authors: Ichise, Shinichiro F and Koide, Takaki
Journal: International Journal of Molecular Sciences (2022): 1584

Interfacing Perforated Eardrums with Graphene-Based Membranes for Broadband Hearing Recovery
Authors: Li, Chunyan and Xiong, Zhiyuan and Zhou, Lei and Huang, Weiluo and He, Yushi and Li, Linpeng and Shi, Haibo and Lu, Jiayu and Wang, Jian and Li, Dan and others,
Journal: Advanced Healthcare Materials (2022): 2201471

References

View all 127 references: Citation Explorer

Improved penile histology by phalloidin stain: circular and longitudinal cavernous smooth muscles, dual-endothelium arteries, and erectile dysfunction-associated changes
Authors: Lin G, Qiu X, F and el TM, Albersen M, Wang Z, Lue TF, Lin CS.
Journal: Urology (2011): 970 e1

Phalloidin perturbs the interaction of human non-muscle myosin isoforms 2A and 2C1 with F-actin
Authors: Diensthuber RP, Muller M, Heissler SM, Taft MH, Chizhov I, Manstein DJ.
Journal: FEBS Lett (2011): 767

pH-(low)-insertion-peptide (pHLIP) translocation of membrane impermeable phalloidin toxin inhibits cancer cell proliferation
Authors: An M, Wijesinghe D, Andreev OA, Reshetnyak YK, Engelman DM.
Journal: Proc Natl Acad Sci U S A (2010): 20246

Labeling cytoskeletal F-actin with rhodamine phalloidin or fluorescein phalloidin for imaging
Authors: Chazotte B., undefined
Journal: Cold Spring Harb Protoc (2010): pdb prot4947

Processing of the phalloidin proprotein by prolyl oligopeptidase from the mushroom Conocybe albipes
Authors: Luo H, Hallen-Adams HE, Walton JD.
Journal: J Biol Chem (2009): 18070

Page updated on October 9, 2024

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Physical properties

Molecular weight	~1800
Solvent	DMSO

Spectral properties

Absorbance (nm)	536
Correction Factor (260 nm)	0.26
Correction Factor (280 nm)	0.16
Extinction coefficient (cm ^-1 M ^-1)	90000¹
Excitation (nm)	537
Emission (nm)	560
Quantum yield	0.68¹

Storage, safety and handling

H-phrase	H301, H311, H331
Hazard symbol	T
Intended use	Research Use Only (RUO)
R-phrase	R23, R24, R25
Storage	Freeze (< -15 °C); Minimize light exposure
UNSPSC	12352200