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PNPLA2 encodes an enzyme which catalyzes the first step in the hydrolysis of triglycerides in adipose tissue. Zusätzlich bieten wir Ihnen Patatin-Like phospholipase Domain Containing 2 Antikörper (176) und Patatin-Like phospholipase Domain Containing 2 Proteine (9) und viele weitere Produktgruppen zu diesem Protein an.
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the ATGL gene plays an important role in triglyceride lipolysis in GMECs; ATGL may be involved in lipid metabolism during lactation
Although we found evidence for moderate association between PNPLA2 tagSNPs and anthropometric and metabolic parameters in our cohort, no evidence for association between polymorphisms in the PNPLA2 gene and the presence and severity of non-alcoholic fatty liver disease was identified.
Study reports the derivation of iPSCs from fibroblasts of two Neutral Lipid Storage Disease with Myopathy (NLSDM)patients carrying different ATGL mutations. These iPSCs exhibited defects in neutral lipid metabolism similar to those of NLSDM fibroblasts. NLSDM-iPSCs were able to undergo directed differentiation into cardiomyocytes.
Thus, ATGL in leucocytes may be an important biomarker for the diagnosis of TGCV and our assay may provide insights into pathophysiology and elucidate the underlying mechanism of TGCV and related disorders.
The ATGL gene was frequently deleted in various forms of human cancers and was associated with poor prognosis.
a Snail1 (zeige SNAI1 ELISA Kits)-ATGL axis that regulates adipose lipolysis and fatty acid release, is reported.
ABHD5 (zeige ABHD5 ELISA Kits) possesses a PNPLA2-independent function in regulating autophagy and tumorigenesis.
Oxidative stress decreased the levels of PNPLA2 transcripts with no effect on ALOX5 expression. Exogenous additions of P1 peptide or overexpression of the PNPLA2 gene decreased both LTB4 levels and death of RPE cells undergoing oxidative stress.
Results suggest that increased adipose triglyceride lipase (ATGL) expression is associated with increased adiposity and stromal proliferation in patients with pancreatic ductal adenocarcinoma (PDAC).
A missense mutation in PNPLA2 is the rare cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease.
A novel deletion was identified in PNPLA2 protein from a patient with complete deficiency of adipose triglyceride lipase.
Loss of ATGL induces spontaneous development of pulmonary neoplasia in knockout mouse model.
ATGL acts as an important upstream signaling node that, via SIRT1 (zeige SIRT1 ELISA Kits), increases autophagy/lipophagy as a means to promote hepatic lipid droplet catabolism.
CGI-58 (zeige ABHD5 ELISA Kits) regulates hepatic neutral lipid storage and inflammation in the genetic absence of ATGL.
Enhanced lipolysis in response to mitochondrial uncoupling relies on a form of autophagy as lipid droplets are captured by endolysosomal vesicles which is HSL (zeige LIPE ELISA Kits)/ATGL-independent.
The Atgl is down-regulated by the basal transcription factor Sp1 (zeige SP1 ELISA Kits) in preadipocytes and that the magnitude of down-regulation depends on interactions between Sp1 (zeige SP1 ELISA Kits) and peroxisome proliferator-activated receptor gamma (PPARgamma (zeige PPARG ELISA Kits)).
TAG synthesis and levels of PUFA-TAGs were lowered by the diacylglycerol acyltransferase (DGAT)1 (zeige DGAT1 ELISA Kits) inhibitor, T863. The lipase (zeige LIPG ELISA Kits) inhibitor, Atglistatin, increased the levels of TAG in both WT and ATGL-deficient mouse Hepatic stellate cell (HSC (zeige FUT1 ELISA Kits)). Both Atglistatin and T863 inhibited the induction of activation marker, alpha-smooth muscle actin (zeige ACTG2 ELISA Kits), in rat HSCs, but not in mouse HSCs.
G0S2 protein but not mRNA levels were reduced in the adipose tissue of ATGL-deficient mice, corroborating the involvement of ATGL in the stabilization of G0S2
Atgl deficiency induces podocyte apoptosis and leads to glomerular filtration barrier damage.
These data raise the possibility that ATGL deficiency could impair the renal fatty acid metabolism though inhibiting PPARalphaexpression, which may lead to lipid deposition and cell apoptosis of PCT (zeige UROD ELISA Kits), and finally contribute to the renal fibrosis and dysfunction
Results identified functional polymorphisms providing new evidence of PNPLA2 as an important candidate gene for fat deposition and carcass traits in pigs.
Resveratrol activated sirtuin 1 (Sirt1 (zeige SIRT1 ELISA Kits)) gene expression and increased adipose triglyceride lipase (ATGL) gene expression and glycerol release. Furthermore, this study found the opposite Sirt1 (zeige SIRT1 ELISA Kits) regulation pattern for PPARgamma (zeige PPARG ELISA Kits) to that of ATGL in adipocytes.
analysis of porcine adipose triglyceride lipase (PNPLA2) gene
JAK (zeige JAK3 ELISA Kits)-STAT (zeige STAT1 ELISA Kits) and MAPK (zeige MAPK1 ELISA Kits) signaling pathways, as well as PPAR gamma (zeige PPARG ELISA Kits) all played important roles in the ATGL expression mediated by leptin (zeige LEP ELISA Kits)
patatin-like phospholipase domain containing 2 gene (PNPLA2) is assiged to chromosome 2 in pigs.
ATGL expression reacts to hormonal stimuli and plays a role in catecholamine-induced lipolysis in porcine adipose tissue.
Tissue distribution of ATGL gene expression was highest in fat and muscle (skeletal and cardiac) tissue, while protein expression was solely detectible in the adipose tissue.
This gene encodes an enzyme which catalyzes the first step in the hydrolysis of triglycerides in adipose tissue. Mutations in this gene are associated with neutral lipid storage disease with myopathy.
patatin-like phospholipase domain-containing protein 2
, patatin-like phospholipase domain containing 2
, adipose triglyceride lipase
, calcium-independent phospholipase A2
, patatin-like phospholipase domain containing protein 2
, pigment epithelium-derived factor
, transport-secretion protein 2.2
, triglyceride hydrolase
, transport-secretion protein