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SAB4200226

Sigma-Aldrich

Anti-PGC-1α(N-terminal) antibody produced in rabbit

enhanced validation

~1.0 mg/mL, affinity isolated antibody

Synonym(s):

Anti-LEM6, Anti-PGC1, Anti-Peroxisome proliferator-activated receptor gamma, coactivator 1 alpha, PPARGC1A

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1 PKG
₩4,43,94,781

About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.41

₩4,43,94,781


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biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~120 kDa

species reactivity

human

enhanced validation

recombinant expression
recombinant expression
Learn more about Antibody Enhanced Validation

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1 of 4

This Item
HPA007266HPA006937HPA006431
biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

rabbit

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

Prestige Antibodies® Powered by Atlas Antibodies

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

General description

PPARG coactivator 1 α (PPARGC1A), a master transcriptional coactivator is a 91kDa multifunctional regulatory factor, encoded by the gene mapped to human chromosome 4p15.1. The encoded protein is mainly expressed in heart, skeletal muscle and kidney.

Application

Anti-PGC-1α(N-terminal) antibody produced in rabbit has been used in immunoblotting.

Biochem/physiol Actions

PPARG coactivator 1 α (PPARGC1α) integrates and regulates several metabolic pathways in response to external stimuli. PGC-1α regulates adaptive thermogenesis in brown adipose tissue and insulin signaling in skeletal muscle by activation of central metabolic and energy-related genes. It has a central role in the regulation of liver gluconeogenesis, β-oxidation of fatty acids and ketogenesis, by coactivation of key enzymes in the metabolic pathway, indicating that PGC-1α plays an important role as a global regulator of liver metabolism during fasting. PGC-1a is also a potent activator of mitochondrial biogenesis by coactivation of estrogen related receptor α(ERRα), nuclear respiratory factors (NRF)-1 and NRF-2. PGC-1a has been shown to suppress the generation of reactive oxygen species (ROS) and neurodegeneration by protecting neuronal cells from oxidative stress-mediated death. PGC-1α has been recently proposed to control muscle plasticity, to suppress broad inflammatory response and mediate the beneficial aspects of exercise.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide

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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Storage Class Code

10 - Combustible liquids

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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    PREDICTION OF SKIN PERMEATION BY CHEMICAL COMPOUNDS USING THE ARTIFICIAL MEMBRANE, STRAT-M?
    Uchida T, Kadhum WR, Kanai S, Todo H, Oshizaka T, Sugibayashi K
    European Journal of Pharmaceutical Sciences null
    IN VITRO SKIN MODELS AS A TOOL IN OPTIMIZATION OF DRUG FORMULATION.
    Flaten GE, Palac Z, Engesland A, Filipovic-Grcic J, Vanic Z, Skalko-Basnet N
    European Journal of Pharmaceutical Sciences null
    IMPACT OF DIFFERENT VEHICLES FOR LASER-ASSISTED DRUG PERMEATION VIA SKIN: FULL-SURFACE VERSUS FRACTIONAL ABLATION.
    Lee WR, Shen SC, Aljuffali IA, Li YC, Fang JY.
    Pharmaceutical Research null
    Membrane properties for permeability testing: Skin versus synthetic membranes
    Haq A, Dorrani M, Goodyear B, Joshi V, Michniak-Kohn B.
    International Journal of Pharmaceutics null
    A REVIEW OF THE CURRENT STATE OF THE ART OF PHYSIOLOGICALLY-BASED TESTS FOR MEASURING HUMAN DERMAL IN VITRO BIOAVAILABILITY OF POLYCYCLIC AROMATIC HYDROCARBONS (PAH) IN SOIL
    Beriro DJ, Cave MR, Wragg J, Thomas R, Wills G, Evans F.
    Journal of Hazardous Materials null

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