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Salicylate activates the AMP-activated protein kinase (AMPK (Montrer PRKAA2 Kits ELISA)) by binding at the A-769662 drug binding site on the AMPK (Montrer PRKAA1 Kits ELISA) beta1-subunit
findings suggest that the reduced expression of AMPK (Montrer PRKAA1 Kits ELISA)-beta1 confers lower AMPK (Montrer PRKAA1 Kits ELISA) activity, which enhances the oncogenic capacity of advanced-stage ovarian cancer.
The effects of ethanol on AMPK (Montrer PRKAA1 Kits ELISA) and PP2A (Montrer PPP2R4 Kits ELISA) may result in activation of ChREBP (Montrer MLXIPL Kits ELISA), providing another potential mechanism for ethanol-induced hepatic steatosis.
Data indicate that a diet high in iron improves glucose tolerance by activating AMPK (Montrer PRKAA1 Kits ELISA) through mechanisms that include deacetylation.
LKB1 (Montrer STK11 Kits ELISA) controls IRS1 (Montrer IRS1 Kits ELISA)-dependent adipogenesis via AMPK (Montrer PRKAA1 Kits ELISA) in white adipose tissue.
Data indicate that except AMPK (Montrer PRKAA1 Kits ELISA)-alpha1, expressions of the other five AMPK (Montrer PRKAA1 Kits ELISA) subunits -alpha2, -beta1, -beta2, -gamma1 and -gamma2 are significantly higher in ovarian carcinomas.
Changes in translational control of mitochondrial proteins are signaled by the activation of AMPK and general control non-derepressible kinase 2 (GCN2), leading also to the activation of autophagy.
Phosphorylation levels of AMPK (Montrer PRKAA1 Kits ELISA) and glycolysis were up-regulated to confer an advantage of survival for MERRF skin fibroblasts.
Adipose tissues of markedly obese insulin (Montrer INS Kits ELISA) resistant individuals uniformly show decreased AMPK (Montrer PRKAA1 Kits ELISA) activity and increased oxidative stress compared with insulin (Montrer INS Kits ELISA) sensitive patients.
In breast cancer cells SESN2 (Montrer SESN2 Kits ELISA) is associated with AMPK (Montrer PRKAA1 Kits ELISA).
In lipid-laden macrophages, Ampk (Montrer PRKAA1 Kits ELISA) activation decreased cholesterol content (foam cell formation) and increased cholesterol efflux to HDL (Montrer HSD11B1 Kits ELISA) and apoA-I (Montrer APOA1 Kits ELISA), effects that occurred in an Ampk (Montrer PRKAA1 Kits ELISA) beta1-dependent manner.
AMPK (Montrer PRKAA1 Kits ELISA) directly relaxes vascular smooth muscle cell by a decrease of [Ca(2 (Montrer CA2 Kits ELISA)+)]i. This is achieved by calcium sequestration via SERCA (Montrer ATP2A3 Kits ELISA) activation, as well as activation of BKCa (Montrer KCNMA1 Kits ELISA) channels.
Norepinephrine increases the expression of PGC-1alpha (Montrer PPARGC1A Kits ELISA) in parallel with the activation of AMPK (Montrer PRKAA1 Kits ELISA) signaling in mouse epididymal adipose tissue.
AMPK (Montrer PRKAA1 Kits ELISA) beta1beta2 have a role in preventing myopathy due to loss of capillary density in nonpostural muscles
PPARbeta (Montrer PPARD Kits ELISA)/delta, but not PPARalpha (Montrer PPARA Kits ELISA), interacts with the exercise-inducible kinase AMP-activated protein kinase (AMPK (Montrer PRKAA2 Kits ELISA)) to synergistically activate Ldhb (Montrer LDHB Kits ELISA) gene transcription by cooperating with myocyte enhancer factor 2A (MEF2A (Montrer MEF2A Kits ELISA)) in a PPARbeta (Montrer PPARD Kits ELISA)/delta ligand-independent manner
The aim of this study was to determine whether activation of AMPK (Montrer PRKAA1 Kits ELISA) by acute renal ischemia influences the severity of renal ischemia-reperfusion injury.
AMPK (Montrer PRKAA1 Kits ELISA) beta1 protects macrophages from inflammation under high lipid exposure from a high fat diet. beta1(-/-) macrophages displayed increased levels of diacylglycerol and markers of inflammation.
cisplatin-triggered activation of AMPK (Montrer PRKAA1 Kits ELISA) and subsequent suppression of mTOR (Montrer FRAP1 Kits ELISA) activity can induce an autophagic response that protects tumour cells from cisplatin-mediated apoptotic death
Phosphorylation of AMPK (Montrer PRKAA1 Kits ELISA) by Ulk1 (Montrer ULK1 Kits ELISA) represents a negative feedback circuit.
The extent of genetic polymorphisms in the promoter region of PRKAB1 gene was investigated in a sample of 811 Chinese indigenous bovine individuals.
Sequence analysis of 811 Chinese indigenous bovine individuals revealed 29 single nucleotide polymorphisms (SNPs) of bovine PRKAB1 gene.
The protein encoded by this gene is a regulatory subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This subunit may be a positive regulator of AMPK activity. The myristoylation and phosphorylation of this subunit have been shown to affect the enzyme activity and cellular localization of AMPK. This subunit may also serve as an adaptor molecule mediating the association of the AMPK complex.
5'-AMP-activated protein kinase subunit beta-1
, AMPK-activated protein kinase beta-1 subunit
, 5'AMP-activated protein kinase beta-1 non-catalytic subunit
, protein kinase, AMP-activated, beta 1 non-catalytic subunit
, AMP-activated protein kinase beta 1 non-catalytic subunit
, AMPK subunit beta-1
, 5'-AMP-activated protein kinase beta-1 subunit
, AMP-activated protein kinase beta subunit
, AMPK beta -1 chain
, AMPK beta 1
, protein kinase, AMP-activated, noncatalytic, beta-1
, 5'-AMP-activated protein kinase 40 kDa subunit
, 5'-AMP-activated protein kinase, beta subunit
, 5-AMP-activated protein kinase beta subunit
, AMPK beta-1 chain