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Dietary fat absorption from the small intestine is facilitated by acyl-CoA:monoacylglycerol transferase (MOGAT\; EC 184.108.40.206) and acyl-CoA:diacylglycerol acyltransferase (DGAT\; see MIM 604900) activities. 再加上，我们可以发MOGAT2 抗体 (40) 和 MOGAT2 蛋白 (5)和数多这个蛋白质的别的产品。
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MGAT2 (显示 MGAT2 ELISA试剂盒) in the intestine plays an indispensable role in enhancing metabolic efficiency but also raise the possibility that MGAT2 (显示 MGAT2 ELISA试剂盒) in other tissues may contribute to the regulation of energy metabolism.
MGAT2 possessed an intrinsic acyl-CoA:diacylglycerol acyltransferase (DGAT) activity which could provide an alternative pathway for triacylglycerol synthesis in the absence of DGAT
Mogat2 is a key determinant of energy metabolism in response to dietary fat and suggest that inhibition or deletion of this enzyme may prove to be a useful strategy for treating obesity.
the release of gut (显示 GUSB ELISA试剂盒) peptides following oral triglyceride ingestion in MGAT2 (显示 MGAT2 ELISA试剂盒) and DGAT1 (显示 DGAT1 ELISA试剂盒) knock-out mice was investigated.
MGAT (显示 MGAT2 ELISA试剂盒)catalyzes the synthesis of diacylglycerol, a precursor of triacylglycerol. MGAT mediates the absorption of dietary fat by catalyzing the resynthesis of triacylglycerol in enterocytes, a step required for delivering absorbed fat to other tissues.
MGAT2 (显示 MGAT2 ELISA试剂盒) is a monoacylglycerol acyltransferase expressed in the small intestine
MGAT2 (显示 MGAT2 ELISA试剂盒) functions as a dimeric or tetrameric protein and selectively heterodimerizes with DGAT1 (显示 DGAT1 ELISA试剂盒) in mammalian cells
Mogat2(IKO) mice increased energy expenditure although to a lesser degree than Mogat2(-/-) mice and were protected against diet-induced weight gain and associated comorbidities
The described cell-based assay adds a new methodology for the development and evaluation of MGAT2 (显示 MGAT2 ELISA试剂盒) inhibitors for the treatment of obesity and type 2 diabetes
Diacylglycerol acyltransferase-2 (显示 AWAT1 ELISA试剂盒) and monoacylglycerol acyltransferase-2 are ubiquitinated proteins that are degraded by the 26S proteasome (显示 Psmd4 ELISA试剂盒)
The use of 1-oleoyl-glycerol-d5 and (U13)C-TG oil followed by LC/ESI (显示 PI3 ELISA试剂盒)/MS/MS detection of stable-isotopic labeled DAG, TG, or glycerol provides a wide range of applications to study pathophysiological regulation of the monoacylglycerol pathway and MGAT2 (显示 MGAT2 ELISA试剂盒) activity.
MGAT2 (显示 MGAT2 ELISA试剂盒) may play an important role in dietary fat absorption
Dietary fat absorption from the small intestine is facilitated by acyl-CoA:monoacylglycerol transferase (MOGAT\; EC 220.127.116.11) and acyl-CoA:diacylglycerol acyltransferase (DGAT\; see MIM 604900) activities. MOGAT catalyzes the joining of monoacylglycerol and fatty acyl-CoAs to form diacylglycerol (Yen and Farese, 2003
2-acylglycerol O-acyltransferase 2
, acyl CoA:monoacylglycerol acyltransferase 2
, monoacylglycerol O-acyltransferase 2
, putative monoacylglycerol acyltransferase 2
, 2-acylglycerol O-acyltransferase 2-like
, acyl-CoA:monoacylglycerol acyltransferase 2
, diacylglycerol acyltransferase 2-like protein 5
, diacylglycerol O-acyltransferase candidate 5
, 2-acylglycerol O-acyltransferase 2-B
, acyl CoA:monoacylglycerol acyltransferase 2-B
, acyl-CoA:monoacylglycerol acyltransferase 2-B
, monoacylglycerol O-acyltransferase 2-B