539573
PKC Inhibitor Set
The PKC Inhibitor Set controls the biological activity of PKC. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
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About This Item
UNSPSC Code:
12352200
NACRES:
NA.77
Quality Level
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
desiccated (hygroscopic)
protect from light
solubility
DMSO: soluble
shipped in
ambient
storage temp.
−20°C
General description
Contains 250 µg of Bisindolylmaleimide I (Cat. No. 203290), 50 µg of Calphostin C, Cladosporium cladosporioides (Cat. No. 208725), 5 mg of Chelerythrine Chloride (Cat. No. 220285), 500 µg of Gö 6976 (Cat. No. 365250), 500 µg of Myristoylated Protein Kinase C Inhibitor 20-28, Cell-Permeable (Cat. No. 476480), and 1 mg of Ro-32-0432 (Cat. No. 557525). Supplied with a data sheet.
Inhibition of protein kinase C (PKC) is one of the most direct methods for investigating its role in cellular metabolism and tumorigenesis. Calbiochem® brand is pleased to offer a convenient set of PKC inhibitors for your research needs. Supplied with a data sheet.
The PKC Inhibitor Set controls the biological activity of PKC. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
Biochem/physiol Actions
Primary Target
PKC
PKC
Secondary Target
PKCα, PKCβ
PKCα, PKCβ
Warning
Toxicity: Multiple Toxicity Values, refer to MSDS (O)
Reconstitution
Following reconstitution, aliquot and freeze -20°C.
Other Notes
Eicholtz, T., et al. 1993. J. Biol. Chem.268, 1982.
Kleinschroth, J., et al. 1993. Bioorg. Med. Chem. Lett.3, 1959.
Martiny-Baron, G.M., et al. 1993. J. Biol. Chem.268, 9194.
Ward, N.E., and O′Brian, C.A. 1993. Biochemistry32, 11903.
Wilkinson, S.E., et al. 1993. Biochem. J.294, 335.
Barg, J., et al. 1992. J. Neurochem.59, 1145.
Gopalakrishna, R., et al. 1992. FEBS Lett.314, 149.
Bruns, R.F., et al. 1991. Biochem. Biophys. Res. Commun.176, 288.
Toullec, D., et al. 1991. J. Biol. Chem.266, 15771.
Herbert, J.M., et al. 1990. Biochem. Biophys. Res. Commun.1172, 993.
Tamaoki, T., et al. 1990. Biotechnology8, 732.
Kobayashi, E., et al. 1989. Biochem. Biophys. Res. Commun.159, 548.
Kleinschroth, J., et al. 1993. Bioorg. Med. Chem. Lett.3, 1959.
Martiny-Baron, G.M., et al. 1993. J. Biol. Chem.268, 9194.
Ward, N.E., and O′Brian, C.A. 1993. Biochemistry32, 11903.
Wilkinson, S.E., et al. 1993. Biochem. J.294, 335.
Barg, J., et al. 1992. J. Neurochem.59, 1145.
Gopalakrishna, R., et al. 1992. FEBS Lett.314, 149.
Bruns, R.F., et al. 1991. Biochem. Biophys. Res. Commun.176, 288.
Toullec, D., et al. 1991. J. Biol. Chem.266, 15771.
Herbert, J.M., et al. 1990. Biochem. Biophys. Res. Commun.1172, 993.
Tamaoki, T., et al. 1990. Biotechnology8, 732.
Kobayashi, E., et al. 1989. Biochem. Biophys. Res. Commun.159, 548.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Regulatory Information
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