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324782 DAPK1, GST-Fusion, Human, Recombinant, S. frugiperda

324782
  
Purchase on Sigma-Aldrich

Overview

Replacement Information
Description
Overview

This product has been discontinued.





Recombinant, human DAPK1 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. DAPK1 is a Ca2+/calmodulin-dependent serine/threonine kinase that acts as a positive regulator of apoptosis.
Catalogue Number324782
Brand Family Calbiochem®
SynonymsDeath-associated protein kinase 1
References
ReferencesBialik, S. and Kimchi, A., 2006. Annu. Rev. Biochem. 75, 189.
Shohat, G., et al. 2001. J. Biol. Chem. 276, 47460.
Deiss, L.P., et al. 1995. Genes Dev. 9, 15.
Product Information
Unit of DefinitionOne unit is defined as the amount of enzyme required to transfer a nmol phosphate to IAKRRRLSSLRASTSKSESSQK peptide substrate per min at 30°C using variable concentrations of ATP (0.1-0.391 µM).
FormLiquid
FormulationIn 100 mM NaCl, 50 mM Tris-HCl, 5 mM DTT, 4 mM reduced glutathione, 20% glycerol, pH 8.0.
Applications
Biological Information
Specific Activity≥50 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
324782 0

Documentation

DAPK1, GST-Fusion, Human, Recombinant, S. frugiperda Certificates of Analysis

TitleLot Number
324782

References

Reference overview
Bialik, S. and Kimchi, A., 2006. Annu. Rev. Biochem. 75, 189.
Shohat, G., et al. 2001. J. Biol. Chem. 276, 47460.
Deiss, L.P., et al. 1995. Genes Dev. 9, 15.
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.

Revision22-August-2007 JSW
SynonymsDeath-associated protein kinase 1
DescriptionRecombinant, human DAPK1 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. DAPK1 is a Ca2+/calmodulin-dependent serine/threonine kinase that acts as a positive regulator of apoptosis.
FormLiquid
FormulationIn 100 mM NaCl, 50 mM Tris-HCl, 5 mM DTT, 4 mM reduced glutathione, 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: R11-IAKRRRLSSLRASTSKSESSQK, 5 µg/50 µl final concentration DAPK1, GST-Fusion, Human, Recombinant, S. frugiperda, diluted in 1X Kinase Dilution Buffer to desired concentration (we use 100 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 DAPK1. 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≥50 U/mg protein
Unit definitionOne unit is defined as the amount of enzyme required to transfer a nmol phosphate to IAKRRRLSSLRASTSKSESSQK peptide substrate per min at 30°C using variable concentrations of ATP (0.1-0.391 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
ReferencesBialik, S. and Kimchi, A., 2006. Annu. Rev. Biochem. 75, 189.
Shohat, G., et al. 2001. J. Biol. Chem. 276, 47460.
Deiss, L.P., et al. 1995. Genes Dev. 9, 15.