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Polyclonal LPIN1 Primary Antibody for IHC (fro), WB - ABIN540690
Péterfy, Phan, Reue: Alternatively spliced lipin isoforms exhibit distinct expression pattern, subcellular localization, and role in adipogenesis. in The Journal of biological chemistry 2005
Show all 3 Pubmed References
Polyclonal LPIN1 Primary Antibody for WB - ABIN540692
Huffman, Mothe-Satney, Lawrence: Insulin-stimulated phosphorylation of lipin mediated by the mammalian target of rapamycin. in Proceedings of the National Academy of Sciences of the United States of America 2002
Show all 3 Pubmed References
Human Polyclonal LPIN1 Primary Antibody for IHC (p), IHC - ABIN189479
Kim, Kim, Koh, Kim, Lee, Chanda, Park, Min, Lee, Park, Choi: Estrogen-related receptor γ (ERRγ) is a novel transcriptional regulator of phosphatidic acid phosphatase, LIPIN1, and inhibits hepatic insulin signaling. in The Journal of biological chemistry 2011
Show all 2 Pubmed References
Dog (Canine) Polyclonal LPIN1 Primary Antibody for ELISA - ABIN4229820
Suviolahti, Reue, Cantor, Phan, Gentile, Naukkarinen, Soro-Paavonen, Oksanen, Kaprio, Rissanen, Salomaa, Kontula, Taskinen, Pajukanta, Peltonen: Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism. in Human molecular genetics 2006
beta-TRCP depletion in HepG2 hepatocellular carcinoma cells (show BTRC Antibodies)resulted in increased Lipin1 protein abundance.
This study showed that LPIN1 knockdown blocks phospholipid synthesis and changes membrane lipid compositions, and that lipin-1 knockdown significantly inhibits tumor growth in vivo using an orthotopic xenograft breast mouse model.
The novel insights into the regulation of human Lipin-1 stability will be useful in planning further studies to elucidate its metabolic processes.
It seems that a new signaling axis, SIRT1 (show SIRT1 Antibodies)-SFRS10 (show TRA2B Antibodies)-LPIN1 axis, acting in the pathogenesis of alcoholic fatty liver disease exists.
Consistent with these observations, LPIN1 levels were positively correlated with IRS1 (show IRS1 Antibodies) expression in human breast cancer. Thus, our results indicate a mechanism by which IRS1 (show IRS1 Antibodies) expression is increased in breast cancer, and LPIN1 may be a promising drug target for anticancer therapy
LPIN1 is upregulated in non-alcoholic fatty liver disease. Up-regulation of miR (show MLXIP Antibodies)-122 can trigger the compensatory response of LPIN1 and CTDNEP1 (show DULLARD Antibodies) in hepatosteatosis.
lipin-1-mediated downregulation of p21 (show CDKN1A Antibodies) is critical for the progress of keratinocyte differentiation
lipin-1 has a critical role in the regulation of macrophage inflammatory responses to modified-LDL
Results of our study suggest that rs2716610: C>T polymorphism of LPIN1 gene could have a protective effect against development of metabolic syndrome, while rs11693809: C>T might affect a glucose control in patients with MS.
Lipin-1 controls main cellular processes involved in cancer progression and that its targeting, alone or in combination with other treatments, could open new avenues in anticancer therapy.
Data suggest that phosphorylation does not affect catalytic activity of lipin 3 (show LPIN3 Antibodies) or its ability to associate with phosphatidic acid in vitro; different polybasic domains in lipin 1 and lipin 3 (show LPIN3 Antibodies) are responsible for phospho-regulation on the former but not the latter enzyme.
Data indicate a critical physiological function of beta-TRCP (show BTRC Antibodies) in regulating hepatic lipid metabolic homeostasis in part through modulating Lipin1 stability.
The insulin resistance induced by lipin-1 downregulation was related to the disturbance of lipid homeostasis. Lipin-1 silencing reduced intracellular DAG and TAG levels, but elevated ceramide accumulation in C2C12 myotubes
Time course analysis demonstrated that the adipogenic 'hub', sampled by PPARgamma (show PPARG Antibodies) and Lpin1, undergoes orchestrated reorganization during adipogenesis.
Our findings provide new insights into the physiological roles of hepatic Lipin1 in systemic energy homeostasis, and suggest that the moderate inactivation of hepatic Lipin1 represents a promising approach for preventing the development of obesity.
c-fos has a role in increasing the catalytic efficiency of lipin 1 beta
reveals a previously unknown role of lipin1 in skeletal muscle regeneration and expands our understanding of the cellular and molecular mechanisms underlying skeletal muscle regeneration
deficits in hepatic PAP (show ASAP1 Antibodies) activity do not impair TG synthesis and accumulation
lipin-1 PAP (show ASAP1 Antibodies) activity functions in autophagy to activate the PKD (show PRKD1 Antibodies)-Vps34 (show PIK3C3 Antibodies) cascade to promote autolysosome maturation.
The lipin1 gene may have a crucial effect on body lipid accumulation in pigs.
Different genotypes of the Lpin1 gene were associated with percentage of leaf fat and intramuscular fat.
The results of this study suggest that suggest that SLC27A6 (show SLC27A6 Antibodies), ACSL1 (show Acsl1 Antibodies), FABP3 (show FABP3 Antibodies), AGPAT6 (show AGPAT6 Antibodies), and LPIN1 coordinately regulate the channeling of fatty acids toward copious milk fat synthesis in bovine mammary.
This gene encodes a magnesium-ion-dependent phosphatidic acid phosphohydrolase enzyme that catalyzes the penultimate step in triglyceride synthesis including the dephosphorylation of phosphatidic acid to yield diacylglycerol. Expression of this gene is required for adipocyte differentiation and it also functions as a nuclear transcriptional coactivator with some peroxisome proliferator-activated receptors to modulate expression of other genes involved in lipid metabolism. Mutations in this gene are associated with metabolic syndrome, type 2 diabetes, and autosomal recessive acute recurrent myoglobinuria (ARARM). This gene is also a candidate for several human lipodystrophy syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their full-length structures have not been determined.
, phosphatidate phosphatase LPIN1-like
, phosphatidate phosphatase LPIN1
, fatty liver dystrophy protein