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Human PPARδ Reporter Assay Kit

SIZE SKU PRICE
1 x-96 well format assays—
3 x-32 assays in-96 well format—
1 x-384 well format assays—
SIZE SKU
1 x-96 well format assays
3 x-32 assays in-96 well format
1 x-384 well format assays

Product Description and Product Data

This is an all-inclusive cell-based luciferase reporter assay kit targeting the Human Peroxisome Proliferator-Activated Receptor Delta. INDIGO’s Human PPAR delta reporter assay utilizes proprietary mammalian cells that have been engineered to provide constitutive expression of the Human PPAR delta. In addition to PPAR delta Reporter Cells, this kit provides two optimized media for use during cell culture and in diluting the user’s test samples, a reference agonist, Luciferase Detection Reagent, and a cell culture-ready assay plate. The principal application of this assay is in the screening of test samples to quantify any functional activity, either agonist or antagonist, that they may exert against human PPAR delta. This kit provides researchers with clear, reproducible results, exceptional cell viability post-thaw, and consistent results lot to lot. Kits must be stored at -80C. Do not store in liquid nitrogen. Note: reporter cells cannot be refrozen or maintained in extended culture.

Features

  • Ready to Use Upon Receipt

  • Includes All Needed Components
  • Contains Transfected Reporter Cells
  • Eliminates Cell Licensing Fees
  • Clear, Reproducible Results
  • Consistent Results Lot to Lot

Product Specifications

Target TypeNuclear Hormone Receptor
SpeciesHuman
Receptor FormHybrid
Assay ModeAgonist, Antagonist
Kit Components
  • PPARd Reporter Cells
  • Cell Recovery Medium (CRM)
  • Compound Screening Medium (CSM)
  • GW0742, (ref. agonist; in DMSO)
  • Detection Substrate
  • Detection Buffer
  • White, sterile, cell-culture ready assay plate
Shelf Life6 months
Orthologs AvailableYes
Shipping RequirementsDry Ice
Storage temperature-80C

Data

Agonist and Antagonist dose-response of the PPARδ receptor. PPARδ reference agonists and antagonists were analyzed. Average Relative Light Units (RLU) and their respective values of Standard Deviation (SD), Coefficient of Variation (CV), Fold-Activation and % Activity were calculated for each treatment concentration (n = 4). Z’ values were calculated as per Zhang, et al. (1999). Data plots were generated using GraphPad Prism software. Compound concentrations were Log transformed and RLU values were normalized to percent (%) activity of the receptor. Non-linear regression analyses were performed and EC50 & IC50 values determined. The large dynamic response and Z’ values confirm the robust performance of the PPARδ agonist and antagonist assays and demonstrate their suitability for use in HTS applications.

Target Background

Peroxisome proliferator-activated receptor delta (PPARδ or PPARβ), also known as NR1C2 is a nuclear receptor encoded by the PPARδ gene. This protein is a potential inhibitor of ligand-induced transcription activity of PPARα and PPARγ. It may function as an integrator of transcription repression and nuclear receptor signaling. The expression of PPARδ gene is found to be elevated in colorectal cancer cells. The elevated expression can be repressed by adenomatosis polyposis coli (APC), a tumor suppressor protein involved in the APC/beta-catenin signaling pathway. Knockout studies in mice suggested the role of PPARδ in myelination of the corpus callosum, epidermal cell proliferation, and glucose and lipid metabolism. PPARδ has been shown to be involved in differentiation, lipid accumulation, directional sensing, polarization, and migration in keratinocytes.

INDIGO’s PPARδ Reporter Assay Systems utilize proprietary mammalian cells engineered to express human PPARδ.

The principle application of this assay product is in the screening of test samples to quantify functional activities, either agonist or antagonist, that they may exert against the human peroxisome proliferator-activated receptor delta.

Citations

Also available as a service

Peroxisome Proliferator-Activated Receptor Delta (PPARd / PPARb, NR1C2)

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