PPARδ is a nuclear hormone receptor that governs a variety of biological processes and may be involved in the development of several chronic diseases, including diabetes, obesity, atherosclerosis, and cancer.In muscle PPAR-β/δ expression is increased by exercise, resulting in increased oxidative (fat-burning) capacity and an increase in type I fibers. Both PPAR-β/δ and AMPK agonists are regarded as exercise mimetics. In adipose tissue PPAR-β/δ increases both oxidation as well as uncoupling of oxidative phosphorylation.PPARδ may function as an integrator of transcription repression and nuclear receptor signaling. It activates transcription of a variety of target genes by binding to specific DNA elements. Well described target genes of PPARδ include PDK4, ANGPTL4, PLIN2, and CD36. The expression of this 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 this protein in myelination of the corpus callosum, epidermal cell proliferation, and glucose and lipid metabolism.This protein has been shown to be involved in differentiation, lipid accumulation, directional sensing, polarization, and migration in keratinocytes.
Background References
暂无
Sequence Similarity
Belongs to the nuclear hormone receptor family. NR1 subfamily.
Tissue Specificity
Ubiquitous with maximal levels in placenta and skeletal muscle.
Western blot analysis of PPAR delta on different lysates with Rabbit anti-PPAR delta antibody (ER1902-24) at 1/1,000 dilution.
Lane 1: SH-SY5Y (Human neuroblastoma cell) cell lysate (10 µg/Lane) Lane 2: NIH/3T3 (Mouse fibroblast) cell lysate (10 µg/Lane) Lane 3: Mouse colon tissue lysate (20 µg/Lane)
Exposure time: 60 seconds; ECL: K1801
Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: ER1902-24, 1/1,000 in 5% BSA, overnight at 4 ℃ Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature
Predicted band size: 50 kDa Observed band size: 50 kDa
Flow cytometric analysis of PPAR delta was done on SHSY5Y cells. The cells were fixed, permeabilized and stained with the primary antibody (ER1902-24, 1/100) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated goat anti-rabbit IgG Secondary antibody at 1/500 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
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