PPAR transcriptional response element (TRE) Clone

PPAR transcriptional response element (TRE) clone for PPAR signaling pathway
PPAR transcriptional response element (TRE) clone for PPAR signaling pathway
Secreted alkaline phosphatase (SEAP)<br />Expression clone
Secreted alkaline phosphatase (SEAP)
Expression clone
Transcriptional response element(TRE) negative control clone
Transcriptional response element(TRE) negative control clone
GAPDH positive control clone
GAPDH positive control clone

PPAR transcriptional response element (TRE) clone for PPAR signaling pathway Secreted alkaline phosphatase (SEAP)
Expression clone
Transcriptional response element(TRE) negative control clone GAPDH positive control clone

Price: $364.00 $411.00 $364.00 $390.00
Catalog#:
  • TR112
  • SEAP-PA01
  • TR001
  • GAPDH-PG02
Size: pEZX-PG02 pEZX-PA01 pEZX-PG02 pEZX-PG02
Qty:
Manual: DownloadDownloadDownload
View your cart


Introduction

GeneCopoeia’s GLuc-ON™ PPAR transcriptional response element (TRE) clone enables analysis of transcriptional activity of peroxisome proliferator-activated receptors (PPARs).  PPARs are a family of three nucleus-localized transcription factors-PPARα, PPARβ/δ, and PPARγ that lead to peroxisome proliferation in response to lipid ligands. PPARs are important players in treatment of various diseases, such as obesity and diabetes.

The GLuc-ON™ PPAR TRE clone contains tandem repeats of PPAR upstream of a minimal promoter and secreted Gaussia luciferase reporter gene, which allows robust and sensitive analysis without lysing the cells.  The PPAR response elements are engineered to provide strong activation with low background (Figure 1). The GLuc-ON™ PPAR TRE clone is provided as transfection-ready DNA. Negative (non-activating), positive (constitutively-activated) ,and normalization (secreted alkaline phosphatase) control clones are also available for purchase.

User Manual
 

Validation Data

Figure 1. Activation of the GLuc-ON™ PPAR TRE by exogenous expression of PPAR. 293T cells were were co-transfected in the presence of 1 µM rosiglitazone with (left to right) negative TRE clone + negative expression clone, negative TRE clone + PPAR expression clone, PPAR TRE clone + negative expression clone, or PPAR TRE clone + PPAR expression clone. Transfected cells were incubated for 40 hours. A Gaussia  Luciferase assay was performed, and transcriptional response activity values are expressed as luminescence fold activation.