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AB133106

PPAR delta Transcription Factor Assay Kit

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(5 Publications)

Abcam's PPAR delta Transcription Factor Assay Kit (ab133106) is a non-radioactive, sensitive method for detecting specific transcription factor DNA binding activity in nuclear extracts.

View Alternative Names

NR1C2, PPARB, PPARD, Peroxisome proliferator-activated receptor delta, PPAR-delta, NUCI, Nuclear hormone receptor 1, Nuclear receptor subfamily 1 group C member 2, Peroxisome proliferator-activated receptor beta, NUC1, PPAR-beta

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Functional Studies - PPAR delta Transcription Factor Assay Kit (AB133106)
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Supplier Data

Functional Studies - PPAR delta Transcription Factor Assay Kit (AB133106)

Panel A : Increasing amounts of positive control (total lysate) are assayed for PPAR delta DNA-binding activity using ab133106.
Panel B : PPAR delta DNA-binding assays are performed in the presence of competitive dsDNA. The decrease in signal caused by addition of competitive dsDNA confirms the assay specificity.

Key facts

Detection method

Colorimetric

Sample types

Nuclear Extracts, Suspension cells, Adherent cells

Reacts with

Mouse, Human

Results type

Semi-Quantitative

Assay Platform

Microplate reader

Product details

Abcam's PPAR delta Transcription Factor Assay Kit (ab133106) is a non-radioactive, sensitive method for detecting specific transcription factor DNA binding activity in nuclear extracts.

A 96-well enzyme-linked immunosorbent assay (ELISA) replaces the cumbersome radioactive electrophoretic mobility shift assay (EMSA). A specific double stranded DNA (dsDNA) sequence containing the peroxisome proliferator response element (PPRE) is immobilized onto the bottom of wells of a 96-well plate. PPARs contained in a nuclear extract, bind specifically to the PPRE. PPAR delta is detected by addition of specific primary antibody directed against PPAR delta. A secondary antibody conjugated to HRP is added to provide a sensitive colorimetric readout at 450 nm. ab133106 detects human PPAR delta.

This assay does not cross-react with PPAR gamma 1 and PPAR gamma 2 or PPAR alpha.

Peroxisome proliferator-activated receptors (PPARs) are ligand activated nuclear receptors. Three PPAR subtypes have been identified: alpha, delta and gamma. PPARs can be activated by polyunsaturated fatty acids, eicosanoids and various synthtic ligands.

PPAR delta is the least understood; however, identification of a high-affinity PPAR delta synthetic ligand suggests a potential role for this receptor in lipid metabolism and obesity. PPAR delta is ubiquitously expressed, but it is particularly abundant in tissues such as liver, intestine, kidney, abdominal adipose, and skeletal muscle.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

What's included?

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Properties and storage information

Shipped at conditions
Dry Ice
Appropriate short-term storage conditions
Multi
Appropriate long-term storage conditions
Multi
Storage information
Please refer to protocols

Product protocols

Target data

Ligand-activated transcription factor key mediator of energy metabolism in adipose tissues (PubMed : 35675826). Receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Has a preference for poly-unsaturated fatty acids, such as gamma-linoleic acid and eicosapentanoic acid. Once activated by a ligand, the receptor binds to promoter elements of target genes. Regulates the peroxisomal beta-oxidation pathway of fatty acids. Functions as transcription activator for the acyl-CoA oxidase gene. Decreases expression of NPC1L1 once activated by a ligand.
See full target information PPARD

Publications (5)

Recent publications for all applications. Explore the full list and refine your search

International journal of molecular sciences 23: PubMed35955783

2022

Cadmium Toxicity Is Regulated by Peroxisome Proliferator-Activated Receptor δ in Human Proximal Tubular Cells.

Applications

Unspecified application

Species

Unspecified reactive species

Chikage Mori,Jin-Yong Lee,Maki Tokumoto,Masahiko Satoh

Cancer discovery 12:2414-2433 PubMed35894778

2022

A Cancer Cell-Intrinsic GOT2-PPARδ Axis Suppresses Antitumor Immunity.

Applications

Unspecified application

Species

Unspecified reactive species

Jaime Abrego,Hannah Sanford-Crane,Chet Oon,Xu Xiao,Courtney B Betts,Duanchen Sun,Shanthi Nagarajan,Luis Diaz,Holly Sandborg,Sohinee Bhattacharyya,Zheng Xia,Lisa M Coussens,Peter Tontonoz,Mara H Sherman

Frontiers in physiology 11:615025 PubMed33408645

2020

Regulation of Peroxisome Proliferator-Activated Receptor Pathway During Torpor in the Garden Dormouse, .

Applications

Unspecified application

Species

Unspecified reactive species

Alexander J Watts,Samantha M Logan,Anna Kübber-Heiss,Annika Posautz,Gabrielle Stalder,Johanna Painer,Kristina Gasch,Sylvain Giroud,Kenneth B Storey

International journal of molecular sciences 21: PubMed32630668

2020

Stearoyl-CoA Desaturase-1 Attenuates the High Shear Force Damage Effect on Human MG63 Osteosarcoma Cells.

Applications

Unspecified application

Species

Unspecified reactive species

Kuo-Chin Huang,Po-Yao Chuang,Rong-Ze Hsieh,Cheng-Nan Chen,Shun-Fu Chang,Yu-Ping Su

PLoS pathogens 10:e1004167 PubMed24945405

2014

The triggering receptor expressed on myeloid cells 2 inhibits complement component 1q effector mechanisms and exerts detrimental effects during pneumococcal pneumonia.

Applications

FuncS

Species

Mouse

Omar Sharif,Riem Gawish,Joanna M Warszawska,Rui Martins,Karin Lakovits,Anastasiya Hladik,Bianca Doninger,Julia Brunner,Ana Korosec,Roland E Schwarzenbacher,Tiina Berg,Robert Kralovics,Jacques Colinge,Ildiko Mesteri,Susan Gilfillan,Andrea Salmaggi,Admar Verschoor,Marco Colonna,Sylvia Knapp
View all publications
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