Finally. Spring is coming 🌷Benefit from a small Easter discount to get your lab ready for brighter, warmer days:5% to 20% Off!
Overview
Protocols
Specifications
Resources
Related Products

Express Full-Length NanoLuc®-Kinase Fusions in Mammalian Cells

The PRKCE-NanoLuc® Fusion Vector contains the coding region of NanoLuc® luciferase fused to the C-terminus of human PRKCE kinase. It is designed for use with the NanoBRET® Target Engagement (TE) Intracellular Kinase Assay, Adherent Format protocol, where the plasmid can be transfected into various cell lines for PRKCE target engagement analysis. The NanoLuc® luciferase kinase fusion vectors are supplied transfection-ready. The CMV promoter drives the expression of the full-length NanoLuc® kinase fusion protein. 

Vector Details:

  • Gene name: PRKCE
  • Sequence
  • Recommended Assay: NanoBRET® TE Intracellular Kinase, K-10
  • Example data using Tracer: K-10

About Kinase Fusion Vector Names

The placement of NanoLuc® either 5´ or 3´ of the kinase gene is optimized for use with NanoBRET® TE Assays and reflected in the vector name. For example, NanoLuc®-kinase implies that NanoLuc® is 5´ to the kinase gene (at the N-terminus of the kinase). Similarly, kinase-NanoLuc® implies NanoLuc® is 3´to the kinase gene (at the C-terminus of the kinase).

NanoBRET® Target Engagement (TE) Intracellular Kinase Assays

The NanoBRET® TE Intracellular Kinase Assays can analyze the affinity of test compounds by competitive displacement of a fluorescent NanoBRET® Tracer reversibly bound to a NanoLuc®-kinase fusion protein in cells. Introduction of competing test compounds results in a dose-dependent decrease in the NanoBRET® signal for estimating intracellular affinity against the target protein. The NanoBRET® Tracer used is determined by your choice of NanoLuc® kinase fusion vector. The Kinase Vector Selection table shows which NanoBRET® Tracer assay is correct for each kinase fusion vector.

Protocols

No protocols available

Specifications

Catalog Number:

Resources

No related resources found

No related products available