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Merck
CN

04-816

Anti-phospho-PPARγ (Ser82) Antibody, clone AW504, rabbit monoclonal

clone AW504, from rabbit

别名:

Nuclear receptor subfamily 1 group C member 3, PPAR gamma, peroxisome proliferative activated receptor gamma, peroxisome proliferator-activated receptor gamma, peroxisome proliferator-activated receptor gamma 1

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UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
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biological source

rabbit

antibody product type

primary antibodies

clone

AW504, monoclonal

species reactivity

mouse, human, rat

technique(s)

western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

shipped in

dry ice

General description

Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors involved in lipid transport and metabolism. As such, their roles in chronic diseases such as diabetes, obesity, atherosclerosis and cancer are heavily investigated. Transcriptional activity of PPARs is regulated by fatty acid binding. Three PPAR isotypes have been identified: ,  and . PPAR stimulates lipolysis of circulating triglycerides and the subsequent uptake of fatty acids into adipose cells. PPARs can bind to DNA only as a heterodimer with the retinoid X receptor (RXR).
~55 & 60 kDa

Immunogen

Epitope: pSer82
KLH-conjugated, synthetic peptide containing the sequence PApSPP in which pS corresponds to phosphoserine at residue 82 of human PPARγ.

Application

Research Category
Epigenetics & Nuclear Function
Research Sub Category
Transcription Factors
Use Anti-phospho-PPAR gamma antibody, clone AW504 (rabbit monoclonal antibody) validated in WB to detect phospho-PPARγ (Ser82) also known as Nuclear receptor subfamily 1 group C member 3 & PPAR gamma.

Biochem/physiol Actions

PPARγ phosphorylated at Ser82, Mr 55 & 60 kDa.
Predicted to cross-react with rat based on sequence homology.

Physical form

Cultured supernantant containing 0.05% sodium azide.
Format: Purified

Preparation Note

Stable for 1 year at -20ºC from date of receipt.
Handling Recommendations: Upon receipt, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

Analysis Note

Control
3T3/L1 cells differentiated into adipocytes, PMA-stimulated THP-1 cells.
Evaluated by western blot on NIH/3T3 L1 cells that were undifferentiated and differentiated into adipocytes.
Western Blot Analysis: 1:500 dilution of this antibody detected PPARγ phosphorylated at Ser82 in undifferentiated and acipocyte differentiated NIH/3T3 L1 cells.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Replaces: 05-816

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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存储类别

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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Jianhui Liu et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 44(2), 423-435 (2017-11-16)
Multiple exposures to anesthesia in children may increase the risk of developing cognitive impairment. Sevoflurane is an anesthetic that is commonly used in children during surgery. Cyclin-dependent kinase (CDK) 5 is involved in the regulation of sevoflurane-induced cognitive dysfunction, but
An ERK/Cdk5 axis controls the diabetogenic actions of PPAR?.
Banks, AS; McAllister, FE; Camporez, JP; Zushin, PJ; Jurczak, MJ; Laznik-Bogoslavski et al.
Nature null
Min-Dian Li et al.
Nature communications, 9(1), 5103-5103 (2018-12-07)
Palatable foods (fat and sweet) induce hyperphagia, and facilitate the development of obesity. Whether and how overnutrition increases appetite through the adipose-to-brain axis is unclear. O-linked beta-D-N-acetylglucosamine (O-GlcNAc) transferase (OGT) couples nutrient cues to O-GlcNAcylation of intracellular proteins at serine/threonine
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Cell stem cell, 28(4), 685-701 (2021-02-05)
Adipose precursor cells (APCs) exhibit regional variation in response to obesity, for unclear reasons. Here, we reveal that HIFα-induced PDGFRβ signaling within murine white adipose tissue (WAT) PDGFRβ+ cells drives inhibitory serine 112 (S112) phosphorylation of PPARγ, the master regulator
Bo Shan et al.
Cell metabolism, 34(5), 783-799 (2022-04-22)
Single-cell RNA sequencing (scRNA-seq) has revealed that adult white adipose tissue (WAT) harbors functionally diverse subpopulations of mesenchymal stromal cells that differentially impact tissue plasticity. To date, the molecular basis of this cellular heterogeneity has not been fully defined. Here

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