Millipore Sigma Vibrant Logo

539573 PKC Inhibitor Set - Calbiochem

The PKC Inhibitor Set controls the biological activity of PKC. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

PKC Inhibitor Set - Calbiochem : FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.

Synonymes: Protein Kinase C Inhibitor Set

Primary Target: PKC
View Products on Sigmaaldrich.com
539573
Voir les Prix & la Disponibilité

Aperçu

Replacement Information

Prix & Disponibilité

Référence DisponibilitéConditionnement Qté Prix Quantité
539573-1SET
Récupération des données relatives à la disponibilité...
—
Disponibilité limitée Disponibilité limitée
En stock 
Interrompu(e)
Disponible en quantités limitées
Disponibilité à confirmer
    Pour le restant : Nous vous tiendrons informé
      Pour le restant : Nous vous tiendrons informé
      Nous vous tiendrons informé
      Contacter le Service Clients
      Contact Customer Service

      		 Flacon en verre 1 set
      Prix en cours de récupération
      Le prix n'a pas pu être récupéré
      La quantité minimale doit être un multiple de
      Maximum Quantity is
      À la validation de la commande Plus d'informations
      Vous avez sauvegardé ()
       
      —
      Demander le prix
      		 —
      Description
      OverviewContains 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.
      Catalogue Number539573
      Brand Family Calbiochem®
      SynonymsProtein Kinase C Inhibitor Set
      Application Data
      References
      ReferencesEicholtz, 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. Biochemistry 32, 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. Biotechnology 8, 732.
      Kobayashi, E., et al. 1989. Biochem. Biophys. Res. Commun. 159, 548.
      Product Information
      FormSolid
      Hygroscopic Hygroscopic
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetPKC
      Secondary targetPKCα, PKCβ
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      R PhraseR: 20/21/22-36/37/38

      Harmful by inhalation, in contact with skin and if swallowed.
      Irritating to eyes, respiratory system and skin.
      S PhraseS: 26-36

      In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
      Wear suitable protective clothing.
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Multiple Toxicity Values, refer to MSDS
      Storage -20°C
      Protect from Light Protect from light
      Hygroscopic Hygroscopic
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Référence GTIN
      539573-1SET 04055977194722

      Documentation

      PKC Inhibitor Set - Calbiochem FDS

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      PKC Inhibitor Set - Calbiochem Certificats d'analyse

      TitreNuméro de lot
      539573

      Références bibliographiques

      Aperçu de la référence bibliographique
      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. Biochemistry 32, 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. Biotechnology 8, 732.
      Kobayashi, E., et al. 1989. Biochem. Biophys. Res. Commun. 159, 548.

      Brochure

      Titre
      Protein Kinase Assay and Detection Kits Brochure
      Fiche technique

      Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

      Revision20-October-2008 JSW
      SynonymsProtein Kinase C Inhibitor Set
      Application Data
      DescriptionInhibition 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.
      FormSolid
      SolubilityThese inhibitors are soluble in DMSO.
      Storage Protect from light
      -20°C
      Hygroscopic
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze -20°C.
      Toxicity Multiple Toxicity Values, refer to MSDS
      ReferencesEicholtz, 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. Biochemistry 32, 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. Biotechnology 8, 732.
      Kobayashi, E., et al. 1989. Biochem. Biophys. Res. Commun. 159, 548.