DGAT1 Rabbit Polyclonal Antibody, 100ul Cell Culture Plates also known as hereditary hyperekplexia

also known as hereditary hyperekplexia or congenital stiff-person syndrome

12-alpha-dihydroxy-4-cholesten-3-one

Knockout studies in mice suggest that this kinase is important for lipopolysaccharide (LPS)-mediated signaling in activated macrophages and may also play a role in controlling anxiety-like behavior

May also be involved in cardiac development

and it is implicated in interstrand-cross-link repair

DGAT1 Rabbit Polyclonal Antibody, 100ul Cell Culture Plates also known as hereditary hyperekplexiaThis gene encodes an multipass transmembrane protein that functions as a key metabolic enzyme. The encoded protein catalyzes the conversion of diacylglycerol and fatty acyl CoA to triacylglycerol. This enzyme can also transfer acyl CoA to retinol. Activity of this protein may be associated with obesity and other metabolic diseases.