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anti-Mouse (Murine) LIPE Antibodies:
anti-Rat (Rattus) LIPE Antibodies:
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Human Polyclonal LIPE Primary Antibody for EIA, FACS - ABIN953181
Bézaire, Mairal, Anesia, Lefort, Langin: Chronic TNFalpha and cAMP pre-treatment of human adipocytes alter HSL, ATGL and perilipin to regulate basal and stimulated lipolysis. in FEBS letters 2009
Show all 5 references for ABIN953181
Human Polyclonal LIPE Primary Antibody for WB - ABIN258047
Kraemer, Patel, Saedi, Sztalryd: Detection of hormone-sensitive lipase in various tissues. I. Expression of an HSL/bacterial fusion protein and generation of anti-HSL antibodies. in Journal of lipid research 1993
Show all 3 references for ABIN258047
Human Polyclonal LIPE Primary Antibody for FACS, IHC (p) - ABIN653323
Drenos, Talmud, Casas, Smeeth, Palmen, Humphries, Hingorani: Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk. in Human molecular genetics 2009
Show all 2 references for ABIN653323
Human Polyclonal LIPE Primary Antibody for IHC, ELISA - ABIN1532302
Holst, Langin, Mulder, Laurell, Grober, Bergh, Mohrenweiser, Edgren, Holm: Molecular cloning, genomic organization, and expression of a testicular isoform of hormone-sensitive lipase. in Genomics 1996
Human Polyclonal LIPE Primary Antibody for EIA, IHC (p) - ABIN500178
Yeaman: Hormone-sensitive lipase--new roles for an old enzyme. in The Biochemical journal 2004
Activities of adipose triglyceride lipase (ATGL (show PNPLA2 Antibodies)), hormone sensitive lipolitic enzyme (HSL) and monoacylglycerol lipase (MGL (show MGLL Antibodies)) were significantly higher (51 %, 38 %, 49 %) in the DE group than the HF group (p < 0.05). MGL (show CLEC10A Antibodies), there were no differences between the CO group, HF group, and DC group, with the DE group (70 %) being significantly higher (p < 0.05).
Results clearly indicate that SF-1 (show SF1 Antibodies) is involved in the regulation of LIPE expression after activation of protein kinase A in adrenocortical cells.
A role for HSL in kidney lipolysis:fasting up-regulates HSL levels and phosphorylation in mouse kidney.
Data suggest that cardiotrophin-1 (show CTF1 Antibodies) up-regulates lipolysis in white adipocytes via 1) induction of perilipin (show PLIN1 Antibodies), 2) activation of HSL (via phosphorylation by PKA), and 3) inactivation of adipose triglyceride lipase (show PNPLA2 Antibodies) (via up-regulation of inhibitor G0S2 (show G0S2 Antibodies)).
QRFP-43 attenuates lipolysis by preventing the formation of an active complex between perilipin A (show PLIN1 Antibodies), caveolin-1 (show CAV1 Antibodies), the catalytic subunit of protein kinase (show CDK7 Antibodies) and hormone-sensitive lipase on lipid droplets.
PRIP (show NCOA6 Antibodies) promotes the translocation of phosphatases to lipid droplets to trigger the dephosphorylation of HSL and perilipin A (show PLIN1 Antibodies), thus reducing PKA-mediated lipolysis.
Whereas the catalytic function of HSL is necessary for spermatogenesis in mice, the presence of the N-terminal testis-specific (show AIF1 Antibodies) fragment is not essential.
Changes in fatty acid metabolism observed in testes from HSL-knockout male mice may underlie the infertility observed in these animals.
HSL acts to drive cAMP/PKA-mediated regulation of StAR expression and steroidogenesis in mouse Leydig cells.
High-fat diet strongly reduced HSL phosphorylation at Ser660 in mouse skeletal muscle.
Despite reductions in intramyocellular lipolysis and HSL expression, overexpression of HSL did not rescue defects in insulin (show INS Antibodies) action in skeletal myotubes from obese type 2 diabetic subjects.
Identification of a homozygous nonsense variant p.Ala507fsTer563 in hormone sensitive lipase as the likely cause of the lipodystrophy phenotype in siblings.
These findings indicate the physiological significance of HSL in adipocyte function and the regulation of systemic lipid and glucose homeostasis and underscore the severe metabolic consequences of impaired lipolysis.
Serum triglyceride was significantly up-regulated in men with the (CG + GG) genotype of HSL promoter polymorphism.
M. leprae suppresses lipid degradation through inhibition of HSL expression.
Enzyme promiscuity in the hormone-sensitive lipase family of proteins.
Resveratrol increased adipose triglyceride lipase (show PNPLA2 Antibodies) gene and protein expressions, an effect that was not observed for hormone-sensitive lipase in human SGBS (show GPC3 Antibodies) adipocytes.
LIPE C-60G variation can inhibit the decrease of LDL-C and the increases of HDL (show HSD11B1 Antibodies)-C and apo A (show APOA Antibodies)-I in young healthy males, and can inhibit the decrease of LDL-C and the increase of insulin (show INS Antibodies) in young healthy females induced by a high-carbohydrate diet.
suggests that genetic variation of HSL may be a risk factor for male infertility
Data show that hormone-sensitive lipase activity is reduced in adipose tissue of patients with and without diabetes, while lipoprotein lipase (show LPL Antibodies) activity is reduces only in patients with diabetes.
Polymorphisms in HSL might be one of important genetic factors that influence carcass yield and meat quality in beef cattle.
These results suggest that HSL was regulated by fatty acids and some hormones in mammary epithelial cells and thereby play an important role of lipid and energy metabolism.
The protein encoded by this gene has a long and a short form, generated by use of alternative translational start codons. The long form is expressed in steroidogenic tissues such as testis, where it converts cholesteryl esters to free cholesterol for steroid hormone production. The short form is expressed in adipose tissue, among others, where it hydrolyzes stored triglycerides to free fatty acids.
, hormone-sensitive lipase
, hormone-sensitive lipase-like
, hormone - sensitive lipase testicular isoform
, lipase E
, hormone-sensitive lipase testicular isoform