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Members of the perilipin family, such as PLIN5, coat intracellular lipid storage droplets and protect them from lipolytic degradation (Dalen et al., 2007 [PubMed 17234449]).[supplied by OMIM, Feb 2010].. Additionally we are shipping Perilipin 5 Kits (4) and Perilipin 5 Proteins (4) and many more products for this protein.
Showing 10 out of 44 products:
Cow (Bovine) Polyclonal PLIN5 Primary Antibody for IHC, IHC (fro) - ABIN258761
Revuelta-López, Cal, Julve, Rull, Martínez-Bujidos, Perez-Cuellar, Ordoñez-Llanos, Badimon, Sanchez-Quesada, Llorente-Cortés: Hypoxia worsens the impact of intracellular triglyceride accumulation promoted by electronegative low-density lipoprotein in cardiomyocytes by impairing perilipin 5 upregulation. in The international journal of biochemistry & cell biology 2015
Show all 3 Pubmed References
Human Polyclonal PLIN5 Primary Antibody for SimWes, WB - ABIN258765
Wolins, Quaynor, Skinner, Tzekov, Croce, Gropler, Varma, Yao-Borengasser, Rasouli, Kern, Finck, Bickel: OXPAT/PAT-1 is a PPAR-induced lipid droplet protein that promotes fatty acid utilization. in Diabetes 2006
Show all 2 Pubmed References
C/EBPalpha (show CEBPA Antibodies) is an essential regulatory factor for perilipin5 transcription and suggest that fasting stimulates perilipin5 transcription through influencing C/EBPalpha (show CEBPA Antibodies) expression.
Notch1 expression is reduced and glu (show G6PC Antibodies)cose-6-phosphatase and (show G6PC Antibodies) perilipin-5 (G6PC/PLIN5) are upr (show NOTCH1 Antibodies)egulated in liver biopsies from nonalcoholic steatohepatitis (NASH) and nonalcoholic fatty liver disease (NAFLD) patients.
High oxygen consumption in middle-aged men was reflected in higher perilipin 5 expression in skeletal muscle.
PLIN5 was significantly colocated with ATGL (show PNPLA2 Antibodies), mitochondria and CGI-58 (show ABHD5 Antibodies), indicating a close association between the key lipolytic effectors in resting skeletal muscle.
Perilipin 5 as a lipid droplet protein adapted to mitochondrial energy utilization
Sprint interval and traditional endurance training increase net intramuscular triglyceride breakdown and expression of perilipin 2 (show PLIN2 Antibodies) and 5
PLIN5 likely plays an important role in intramyocellular lipid accumulation and oxidation, both of which increase with endurance training in human skeletal muscle.
The lipid droplet coat protein (show GOLPH3 Antibodies) perilipin 5 also localizes to muscle mitochondria.
Perilipin 5 is the most recently established family member, highly expressed in oxidative tissues and could play an important role in regulating LD TAG hydrolysis in oxidative mammalian tissues. [Review]
interaction of ATGL (show PNPLA2 Antibodies) with CGI-58 (show ABHD5 Antibodies) increased lipolysis, whereas interaction of ATGL (show PNPLA2 Antibodies) with perilipin 5 decreased lipolysis.
Results indicate involvement of OXPAT and ADRP (show PLIN2 Antibodies) in muscular lipid accumulation and type 2 diabetes.
mitochondria isolated from hearts deficient in Plin5, have specific functional defects
Plin5 deficiency alters cardiac lipid metabolism and associates with reduced survival following myocardial ischemia.
Data show that glucose-6-phosphatase (show G6PC Antibodies) and perilipin-5 (G6PC (show G6PC Antibodies)/PLIN5) are upregulated in notch1 (show NOTCH1 Antibodies) knockout (KO) mice.
PLIN5 is dispensable for normal substrate metabolism during exercise and is not required to promote mitochondrial biogenesis or enhance the cellular adaptations to endurance exercise training.
High fat diet-induced liver fibrosis is accompanied by an approximate 75% reduction in Plin5 in hepatic stellate cells (HSC (show FUT1 Antibodies)), and spontaneous activation of primary HSC (show FUT1 Antibodies) produces temporally coincident loss of Plin5 expression and lipid droplet depletion.
Here, we identify synthetic ligands that release ABHD5 (show ABHD5 Antibodies) from PLIN1 (show PLIN1 Antibodies) or PLIN5 without PKA activation and rapidly activate adipocyte and muscle lipolysis.
the increase in liver PLIN5 during hepatosteatosis drives further lipid accumulation but does not adversely affect hepatic health or insulin (show INS Antibodies) sensitivity.
upregulating the PLIN5 level in skeletal muscle drives expression of the FGF21 (show FGF21 Antibodies) gene in fast-twitch fibers and is metabolically protective.
the elevation of islet PLIN5 during fasting allows partitioning of fatty acids into lipid droplets that is released upon refeeding to support postprandial insulin (show INS Antibodies) secretion in cAMP- and GPR40 (show FFAR1 Antibodies)-dependent manners.
protein kinase A and perilipin 5 interact to regulate cardiac lipolysis
Members of the perilipin family, such as PLIN5, coat intracellular lipid storage droplets and protect them from lipolytic degradation (Dalen et al., 2007
lipid storage droplet protein 5
, perilipin 5
, lipid droplet associated protein
, lipid droplet-associated protein PAT-1
, myocardial LD protein