
Phorbol Esters(PMA)
Attention: the price only for your reference, the detail price pleasecontact our seller Vecent.
Description
| SKU-Pack Size | Availability | Price |
| abs9107-1mg | 1-2 weeks | $267.00 |
| abs9107-5mg | In stock | $627.00 |
| abs9107-25mg | In stock | $1881.00 |
Attention: the price only for your reference, the detail price pleasecontact our seller Vecent.
Description | |
| Description | Derived from croton oil, PMA (Phorbol-12-Myristate-13-Acetate) is a diester of phorbol and acts as a potent protein kinase C (PKC) activator. It promotes tumor growth in a reversible manner, making it a highly significant compound in the study of cancer. As a diacylglycerol mimic, PMA is known to activate PKC by binding to its regulatory domain. This property makes it a key tool in the study of PKC-mediated signal transduction pathways. Overall, PMA is an essential component of research aimed at understanding cancer cell biology and developing effective treatments for the disease.in vitro and in vivoAt nM concentrations, PMA can activate protein kinase C (PKC) due to its similarity to diacylglycerol, which is a natural activator of PKC. This activation of PKC is believed to be caused by PMA's similarity to diacylglycerol. Additionally, PMA is known to activate Ca2+.2+This particular compound, known as PMA, has been found to have a significant impact on various cellular processes. It is a potent activator of protein kinase C and can increase the production of inositol phosphates. In addition, PMA has been shown to increase the activity of a type of ATPase enzyme, which helps to generate energy for the cell. |
| Applications | A highly potent activator of protein kinase C (PKC) that is both reversible and reversible can be generated by rearranging the provided content. |
| Purity | ≥98% |
| Storage Temp. | Store at -20° C,3 years. |
Properties | |
| Synonym | Phorbol-12-Myristate-13-Acetate, also known as TPA, is a chemical compound that is used in various medical and scientific research applications. Another name for TPA is 12-O-tetradecanoyl phorbol-13-acetate. This chemical compound is commonly used to stimulate the activity of certain protein kinase enzymes in cells, which can be useful for studying cell signaling pathways and other biological processes. Despite its potential benefits for research, TPA is also known to have toxic effects and must be handled with caution. Researchers should be aware of these risks and take appropriate precautions when working with this compound. |
| Appearance | White Powder |
| Solubility | This substance exhibits solubility in various organic solvents such as DMSO (25 mg/ml), 100% ethanol (25 mg/ml), acetone, ether, DMF, methanol, and chloroform. However, it does not dissolve in water or aqueous buffers. |
References | |
| References | The article titled "J. Biol. Chem. 257: 7847-7851" by Castagna et al. published in 1982 provides valuable insights into a specific topic. The article's PMID is 7085651 and serves as a helpful reference for readers interested in learning more about this subject. By rearranging the original text information, we can create a highly similar content that conveys the same message. Sure, here's a highly similar rearranged content based on the original information: The study conducted by Beguinot and colleagues in 1985, published in the Proceedings of the National Academy of Sciences, focused on a specific topic. Their research aimed to investigate a particular phenomenon, and they presented their findings in the article with the reference PMID: 2859591. The study involved gathering data and analyzing it to draw conclusions about the subject at hand. Their work contributed valuable insights to the scientific community and added to the existing knowledge on the topic. 3. Saltis, J., et al. 1991. J. Biol. Chem. 266: 261-267. PMID: 1985898 4. Zanaboni, P.B., et al. 1992. J. Appl. Physiol. 73: 2011-2015. PMID: 1474079 5. Oishi, K. and Yamaguchi, M. 1994. J. Cell. Biochem. 55: 168-172. PMID: 8089192 6. Tepper, C.G., et al. 1995. Proc. Natl. Acad. Sci. U.S.A. 92: 8443-8447. PMID: 7545303 7. Powell, D.J., et al. 2003. Mol. Cell. Biol. 23: 7794-7808. PMID: 14560023 8. Saraiva, L., et al. 2004. Eur. J. Pharmacol. 491: 101-110. PMID: 15140626 9. Shimura, C., et al. 2010. Am. J. Pathol. 176: 227-237. PMID: 20008150 |
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