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324784 ErbB2, GST-Fusion, Human, Recombinant, S. frugiperda

ErbB2, GST-Fusion, Human, Recombinant, S. frugiperda MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: Receptor tyrosine-protein kinase erbB-2, Tyrosine kinase-type cell surface receptor HER2, v-erb-b2 erythroblastic leukemia viral oncogene homolog 2

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      Overview

      Replacement Information
      Description
      OverviewRecombinant, human ErbB2 fused at the N-terminus to a GST-thrombin cleavage site sequence and expressed in S. frugiperda insect cells using a baculovirus expression system. ErbB2 is a component of a neuregulin-receptor complex that regulates neuromuscular synapse formation. It plays an important role in muscle spindle development. Overexpression of ErbB2 is reported in ~30% of all breast cancer cases. Amino acid sequence human ERB2 679-1255.
      Catalogue Number324784
      Brand Family Calbiochem®
      SynonymsReceptor tyrosine-protein kinase erbB-2, Tyrosine kinase-type cell surface receptor HER2, v-erb-b2 erythroblastic leukemia viral oncogene homolog 2
      References
      ReferencesAmin, D.N., et al. 2004. Oncogene 23, 1428;. Vernimmen, D., et al. 2003. J. Cancer 89, 899. Ozcelik, C., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 8880. Coussens, L., et al. 1985 Science 230, 1132.
      Product Information
      Unit of DefinitionOne unit is defined as the amount of enzyme that will transfer 1 nmol phosphate to Poly(Glu,Tyr)<sub>4:1</sub> per min at 30°C using variable concentrations of ATP (100 nM to 5.8 µM).
      FormLiquid
      FormulationIn 100 mM NaCl, 50 mM Tris-HCl, 15 mM reduced glutathione, 5 mM DTT, 20% glycerol, pH 8.0.
      Applications
      Biological Information
      Specific Activity≥20 U/mg 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
      Catalogue Number GTIN
      324784 0

      Documentation

      ErbB2, GST-Fusion, Human, Recombinant, S. frugiperda Certificates of Analysis

      TitleLot Number
      324784

      References

      Reference overview
      Amin, D.N., et al. 2004. Oncogene 23, 1428;. Vernimmen, D., et al. 2003. J. Cancer 89, 899. Ozcelik, C., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 8880. Coussens, L., et al. 1985 Science 230, 1132.
      Data Sheet

      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.

      Revision27-January-2010 RFH
      SynonymsReceptor tyrosine-protein kinase erbB-2, Tyrosine kinase-type cell surface receptor HER2, v-erb-b2 erythroblastic leukemia viral oncogene homolog 2
      DescriptionRecombinant, human ErbB2 fused at the N-terminus to a GST-thrombin cleavage site sequence and expressed in S. frugiperda insect cells using a baculovirus expression system. ErbB2 is a component of a neuregulin-receptor complex that regulates neuromuscular synapse formation. It plays an important role in muscle spindle development. Overexpression of ErbB2 is reported in ~30% of all breast cancer cases. Amino acid sequence human ERB2 679-1255.
      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: Poly(Glu,Tyr)4:1, 250 ng/50 µl final concentration • ErbB2, GST-Fusion, Human, Recombinant, S. frugiperda, diluted in 1X Kinase Dilution Buffer to desired concentration (we use 200 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 ErbB2. 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.
      Specific activity≥20 U/mg protein
      Unit definitionOne unit is defined as the amount of enzyme that will transfer 1 nmol phosphate to Poly(Glu,Tyr)4:1 per min at 30°C using variable concentrations of ATP (100 nM to 5.8 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
      ReferencesAmin, D.N., et al. 2004. Oncogene 23, 1428;. Vernimmen, D., et al. 2003. J. Cancer 89, 899. Ozcelik, C., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 8880. Coussens, L., et al. 1985 Science 230, 1132.