CCCP
Tocris Bioscience | Catalog # 0452
Key Product Details
Description
Product Description
CCCP is a protonophore. It disrupts mitochondria membrane potential by transporting protons across the mitochondrial inner membrane, which interferes with the proton gradient and ATP synthesis. CCCP is a widely used as an uncoupler of oxidative phosphorylation to induce mitochondrial depolarization.
Product Specifications for CCCP
Molecular Weight
Formula
Storage
Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 20.46 | 100 |
Preparing Stock Solutions for CCCP
The following data is based on the product molecular weight 204.62.
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 4.89 mL | 24.44 mL | 48.87 mL |
| 5 mM | 0.98 mL | 4.89 mL | 9.77 mL |
| 10 mM | 0.49 mL | 2.44 mL | 4.89 mL |
| 50 mM | 0.10 mL | 0.49 mL | 0.98 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 34 publications citing the usage of this product.
- Heytler and Pritchard A new class of uncoupling agents - carbonyl cyanide phenylhydrazones. Biochem.Biophys.Res.Commun. 1962 PMID: 13907155
Product Documents for CCCP
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for CCCP
For research use only
Citations for CCCP
Customer Reviews for CCCP (1)
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Customer Images
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Species: RatAssay Type: In VitroCell Line/Tissue: spinal cord neuronsVerified Customer | Posted 10/24/2018Time lapse images of TMRM fluorescence of mitochondria rich regions in neurons was recorded. The fluorescence intensity (F) at a given time point was normalized to the initial fluorescence intensity (F0) before addition of the AMPA. At the end of each experiment CCCP (750 nM) was added to the bath. CCCP collapses the mitochondrial membrane potential and decreases the TMRM fluorescence.TMRM fluorescence intensity before and after CCCP addition was used for the quantitation of change in mitochondrial membrane potential in spinal cord neurons induced by glutamate receptor agonist AMPA
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