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7815
HTScan® PKCε Kinase Assay Kit
Cellular Assay Kits
Assay Kit

HTScan® PKCε Kinase Assay Kit #7815

Citations (0)
HTScan® PKCε Kinase Assay Kit: Image 1

Figure 3. Dose dependence curve of PKCepsilon kinase activity: DELFIA® data generated using Phospho-PKA Substrate (RRXS/T) (100G7) Rabbit mAb #9624 to detect phosphorylation of substrate peptide (#1331) by PKCepsilon kinase. In a 50 µl reaction, increasing amounts of PKCepsilon and 1.5 µM substrate peptide were used per reaction at room temperature for 15 minutes. (DELFIA® is a registered trademark of PerkinElmer, Inc.)

HTScan® PKCε Kinase Assay Kit: Image 2

Figure 5. Staurosporine inhibition of PKCepsilon kinase activity: DELFIA® data generated using Phospho-PKA Substrate (RRXS/T) (100G7) Rabbit mAb #9624 to detect phosphorylation of PKCepsilon substrate peptide (#1331) by PKCepsilon kinase. In a 50 µl reaction, 25 ng PKCepsilon, 1.5 µM substrate peptide, 20 µM ATP and increasing amounts of staurosporine were used per reaction at room temperature for 15 minutes. (DELFIA® is a registered trademark of PerkinElmer, Inc.)

HTScan® PKCε Kinase Assay Kit: Image 3

Figure 4. Peptide concentration dependence of PKCepsilon kinase activity: DELFIA® data generated using Phospho-PKA Substrate (RRXS/T) (100G7) Rabbit mAb #9624 to detect phosphorylation of substrate peptide (#1331) by PKCepsilon kinase. In a 50 µl reaction, 25 ng of PKCepsilon and increasing concentrations of substrate peptide were used per reaction at room temperature for 15 minutes. (DELFIA® is a registered trademark of PerkinElmer, Inc.)

HTScan® PKCε Kinase Assay Kit: Image 4

Figure 2. Time course of PKCepsilon kinase activity: DELFIA® data generated using Phospho-PKA Substrate (RRXS/T) (100G7) Rabbit mAb #9624 to detect phosphorylation of PKCepsilon substrate peptide (#1331) by PKCepsilon kinase. In a 50 µl reaction, 25 ng PKCepsilon and 1.5 µM substrate peptide were used per reaction. (DELFIA® is a registered trademark of PerkinElmer, Inc.)

HTScan® PKCε Kinase Assay Kit: Image 5

Figure 1. PKCepsilon kinase activity was measured in a radiometric assay using the following reaction conditions: 4 mM MOPS, pH 7.2, 2.5 mM β-glycerophosphate, 1 mM EGTA, 0.4 mM EDTA, 4 mM MgCl2, 0.05 mM DTT, 40 ng/μl BSA, 50 μg/ml phosphatidylserine, 5 μg/ml diacylglycerol, 0.1 mM sodium orthovanadate, 0.1 mM dithioreitol, 0.1 mM CaCl2, 50 μM ATP, Substrate: PKCepsilon substrate peptide 300 ng/μL and recombinant PKCepsilon: variable.

To Purchase # 7815

Product Description

The kit provides a means of performing kinase activity assays with recombinant human PKCepsilon kinase. It includes active PKCepsilon kinase (supplied as a GST fusion protein), a biotinylated peptide substrate and a phospho-serine/threonine antibody for detection of the phosphorylated form of the substrate peptide.

Molecular Formula

Peptide substrate, Biotin-peptide: 2,326 Daltons. GST-PKCepsilon Kinase domain: 110 kDa.

Background

Activation of protein kinase C (PKC) is one of the earliest events in a cascade that controls a variety of cellular responses, including secretion, gene expression, proliferation, and muscle contraction (1,2). PKC isoforms belong to three groups based on calcium dependency and activators. Classical PKCs are calcium-dependent via their C2 domains and are activated by phosphatidylserine (PS), diacylglycerol (DAG), and phorbol esters (TPA, PMA) through their cysteine-rich C1 domains. Both novel and atypical PKCs are calcium-independent, but only novel PKCs are activated by PS, DAG, and phorbol esters (3-5). Members of these three PKC groups contain a pseudo-substrate or autoinhibitory domain that binds to substrate-binding sites in the catalytic domain to prevent activation in the absence of cofactors or activators. Control of PKC activity is regulated through three distinct phosphorylation events. Phosphorylation occurs in vivo at Thr500 in the activation loop, at Thr641 through autophosphorylation, and at the carboxy-terminal hydrophobic site Ser660 (2). Atypical PKC isoforms lack hydrophobic region phosphorylation, which correlates with the presence of glutamic acid rather than the serine or threonine residues found in more typical PKC isoforms. The enzyme PDK1 or a close relative is responsible for PKC activation. A recent addition to the PKC superfamily is PKCμ (PKD), which is regulated by DAG and TPA through its C1 domain. PKD is distinguished by the presence of a PH domain and by its unique substrate recognition and Golgi localization (6). PKC-related kinases (PRK) lack the C1 domain and do not respond to DAG or phorbol esters. Phosphatidylinositol lipids activate PRKs, and small Rho-family GTPases bind to the homology region 1 (HR1) to regulate PRK kinase activity (7).

PKCepsilon regulates various physiological functions and is involved in the activation of nervous, endocrine, exocrine, inflammatory and immune systems. Disruption of PKCepsilon regulation has been related to diseases including cardiac ischemia, Alzheimer’s, malignant tumors and diabetes (10).

  1. Nishizuka, Y. (1984) Nature 308, 693-8.
  2. Keranen, L.M. et al. (1995) Curr Biol 5, 1394-403.
  3. Mellor, H. and Parker, P.J. (1998) Biochem J 332 ( Pt 2), 281-92.
  4. Ron, D. and Kazanietz, M.G. (1999) FASEB J 13, 1658-76.
  5. Moscat, J. and Diaz-Meco, M.T. (2000) EMBO Rep 1, 399-403.
  6. Baron, C.L. and Malhotra, V. (2002) Science 295, 325-8.
  7. Flynn, P. et al. (2000) J Biol Chem 275, 11064-70.
  8. Akita, Y. (2002) J. Biochem. (Tokyo) 132, 847-852.

Pathways & Proteins

Explore pathways + proteins related to this product.

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For Research Use Only. Not For Use In Diagnostic Procedures.
Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
DELFIA is a registered trademark of PerkinElmer, Inc.