Date published: 2025-11-27

1-800-457-3801

SCBT Portrait Logo
Seach Input

Phalloidin-tetramethylrhodamine conjugate

5.0(1)
Write a reviewAsk a question

See product citations (8)

Application:
Phalloidin-tetramethylrhodamine conjugate is a fluorescent phallotoxin that can be used to identify filamentous actin
Molecular Weight:
~1300
Molecular Formula:
C60H70O14N11S
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Phalloidin-tetramethylrhodamine conjugate is a chemically synthesized compound where phalloidin, a bicyclic peptide derived from the toxic Amanita phalloides mushroom, is conjugated with tetramethylrhodamine, a fluorescent dye. This conjugation enhances the utility of phalloidin in biological research, particularly in the study of cytoskeletal structures. Phalloidin itself binds with high specificity and affinity to F-actin, a filamentous form of actin, thereby stabilizing these filaments and preventing their depolymerization. The incorporation of tetramethylrhodamine introduces a fluorescent property to the molecule, enabling researchers to visualize actin filaments within cells using fluorescence microscopy techniques. This is particularly useful in cell biology, where understanding the structure, organization, and dynamics of the cytoskeleton is crucial. Through the fluorescence emitted by tetramethylrhodamine, scientists can track the distribution and organization of actin filaments in live or fixed cells and tissues, providing insights into cellular architecture and the mechanics of cell movement and division. The conjugate′s specificity for F-actin and its bright, photostable fluorescence make it an indispensable tool in advanced imaging applications, contributing significantly to elucidating molecular pathways that govern cytoskeletal function and cellular processes.


Phalloidin-tetramethylrhodamine conjugate References

  1. Multiple spectral parameter imaging.  |  Waggoner, A., et al. 1989. Methods Cell Biol. 30: 449-78. PMID: 2648118
  2. MicroRNA‑1 suppresses cardiac hypertrophy by targeting nuclear factor of activated T cells cytoplasmic 3.  |  Yin, H., et al. 2015. Mol Med Rep. 12: 8282-8. PMID: 26497337
  3. Wnt5a and CCL25 promote adult T-cell acute lymphoblastic leukemia cell migration, invasion and metastasis.  |  Deng, X., et al. 2017. Oncotarget. 8: 39033-39047. PMID: 28380463
  4. Cholesterol-Modified Caged siRNAs for Photoregulating Exogenous and Endogenous Gene Expression.  |  Yang, J., et al. 2018. Bioconjug Chem. 29: 1010-1015. PMID: 29513987
  5. The effect of lncRNA-ARAP1-AS2/ARAP1 on high glucose-induced cytoskeleton rearrangement and epithelial-mesenchymal transition in human renal tubular epithelial cells.  |  Li, L., et al. 2020. J Cell Physiol. 235: 5787-5795. PMID: 31975379
  6. Matrix Stiffness Potentiates Stemness of Liver Cancer Stem Cells Possibly via the Yes-Associated Protein Signal.  |  Li, H., et al. 2022. ACS Biomater Sci Eng. 8: 598-609. PMID: 35084830
  7. Hyperoside suppresses osteoclasts differentiation and function through downregulating TRAF6/p38 MAPK signaling pathway.  |  Zhu, J., et al. 2022. J Asian Nat Prod Res. 24: 1157-1168. PMID: 35435096
  8. Preparation of tetramethylrhodaminyl-phalloidin and uptake of the toxin into short-term cultured hepatocytes by endocytosis.  |  Faulstich, H., et al. 1983. Exp Cell Res. 144: 73-82. PMID: 6840214
  9. Magnetic poly (ε-caprolactone)-based nanocomposite membranes for bone cell engineering  |  Świętek, M., Brož, A., Kołodziej, A., Hodan, J., Tokarz, W., Hlukhaniuk, A., Wesełucha-Briczyńska, A., Bačáková, L. and Horák, D. 2022. Journal of Magnetism and Magnetic Materials. 563: 169967.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Phalloidin-tetramethylrhodamine conjugate, 300 tests

sc-362065
300 tests
$204.00