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325890 PAK2, GST-Fusion, Human, Recombinant, S. frugiperda

FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.

Synonymes: p21 (CDKN1A)-activated kinase 2, p21-activated kinase 2

325890
  
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      Aperçu

      Replacement Information
      Description
      OverviewRecombinant, human p21-activated protein kinase 2 (PAK2) fused at the N-terminus to a GST-His6-thrombin cleavage site sequence and expressed in S. frugiperda insect cells using a baculovirus expression system. PAK2 is a member of the STE20 subfamily of serine/threonine kinases. It interacts with GTP-bound, but not GDP-bound, CDC42/p21 and RAC1. PAK2 plays an important role in cell signaling pathways that control cell growth, shape, motility, survival, and death. It phosphorylates ribosomal protein S6, histone H4, and myelin basic protein.
      Catalogue Number325890
      Brand Family Calbiochem®
      Synonymsp21 (CDKN1A)-activated kinase 2, p21-activated kinase 2
      References
      ReferencesKoeppel, M.A., et al. 2004. J. Biol. Chem. 279, 53653. Wu, H. and Wang, Z.X. 2003. J. Biol. Chem. 278, 41768. Martin, G.A., et al. 1995. EMBO J. 14, 1970
      Product Information
      Unit of DefinitionOne unit is defined as the amount of enzyme required to transfer 1 pmol phosphate to tetra(LRRWSLG) per min at 30°C using variable concentrations of ATP (100 nM to 36.8 µM).
      EC number2.7.1.37
      FormLiquid
      FormulationIn 100 mM NaCl, 50 mM Tris-HCl, 15 mM reduced glutathione, 5 mM DTT, 20% glycerol, pH 8.0.
      Applications
      Biological Information
      Purity≥95% by SDS-PAGE
      Specific Activity≥193 U/µg protein
      Concentration Label Please refer to vial label for lot-specific concentration
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Dry Ice Only
      Toxicity Standard Handling
      Storage ≤ -70°C
      Avoid freeze/thaw Avoid freeze/thaw
      Do not freeze Ok to freeze
      Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Référence GTIN
      325890 0

      Documentation

      PAK2, GST-Fusion, Human, Recombinant, S. frugiperda Certificats d'analyse

      TitreNuméro de lot
      325890

      Références bibliographiques

      Aperçu de la référence bibliographique
      Koeppel, M.A., et al. 2004. J. Biol. Chem. 279, 53653. Wu, H. and Wang, Z.X. 2003. J. Biol. Chem. 278, 41768. Martin, G.A., et al. 1995. EMBO J. 14, 1970
      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.

      Revision23-August-2007 JSW
      Synonymsp21 (CDKN1A)-activated kinase 2, p21-activated kinase 2
      DescriptionRecombinant, human p21-activated protein kinase 2 (PAK2) fused to a GST-His6-thrombin cleavage site sequence at the N-terminus and expressed in S. frugiperda insect cells using a baculovirus expression system. PAK2 is a member of the STE20 subfamily of serine/threonine kinases. It interacts with GTP-bound, but not GDP-bound, CDC42/p21 and RAC1. PAK2 plays an important role in cell signaling pathways that control cell growth, shape, motility, survival, and death. It phosphorylates ribosomal protein S6, histone H4, and myelin basic protein.
      FormLiquid
      FormulationIn 100 mM NaCl, 50 mM Tris-HCl, 15 mM reduced glutathione, 5 mM DTT, 20% glycerol, pH 8.0.
      Concentration Label Please refer to vial label for lot-specific concentration
      Recommended reaction conditions
      96-Well Membrane Binding Kinase Activity Assay Protocol:
      Materials Required • Standard Kinase Assay Buffer: 125 mM HEPES-NaOH, 7.5 mM MgCl2, 7.5 mM MnCl2, 7.5 µM sodium -orthovanadate, 2.5 mM DTT, pH 7.5 • 10X Kinase Dilution Buffer: 500 mM HEPES-NaOH, 2.5 mg/ml PEG20.000, 10 mM DTT, pH 7.5 • Substrate: Tetra(LRRWSLG), 5 µg/50 µl final concentration • PAK2, GST-Fusion, Human, Recombinant, S. frugiperda, diluted in 1X Kinase Dilution Buffer to desired concentration (we use 50 ng in a 50 µl reaction) • 33P-γ-ATP • ATP Mix: 1 µM ATP in H2O with 1 x 106 cpm/5 µl • 96-well V-bottom MTP (polypropylene) plates (Nunc Cat. No. 442587) • 96-well Multiscreen Vacuum Manifold (Millipore Cat. No. MAVM096OR) • 96-well Multiscreen Filterplates, phosphocellulose membrane (Millipore Cat. No. MSPH N6B50) and glass fiber (Millipore Cat. No. MSFC N6B50) • 2% H3PO4 • 0.9% NaCl
      Activity Assay Protocol 1. In a polypropylene V-bottom plate add 20 µl Kinase Assay Buffer 2. If desired, add 5 µl test substance (e.g., inhibitor, activator, etc.; in 10% DMSO) 3. Add 10 µl Substrate (diluted in H2O). 4. Add 10 µl diluted PAK2. 5. Add 5 µl ATP Mix. 6. Mix on a shaker and incubate at 30°C for 80 min. 7. Stop the reaction with 50 µl H3PO4. 8. Prewet the filter plate with 200 µl H2O. 9. Filter the reaction mix by applying vacuum. 10. Wash 3 times with 200 µl 0.9% NaCl. 11. Add 200 µl scintillation fluid to each well and count on a scintillation counter.
      EC number2.7.1.37
      Purity≥95% by SDS-PAGE
      Specific activity≥193 U/µg protein
      Unit definitionOne unit is defined as the amount of enzyme required to transfer 1 pmol phosphate to tetra(LRRWSLG) per min at 30°C using variable concentrations of ATP (100 nM to 36.8 µM).
      Storage Avoid freeze/thaw
      ≤ -70°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
      Toxicity Standard Handling
      ReferencesKoeppel, M.A., et al. 2004. J. Biol. Chem. 279, 53653. Wu, H. and Wang, Z.X. 2003. J. Biol. Chem. 278, 41768. Martin, G.A., et al. 1995. EMBO J. 14, 1970