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The protein encoded by AGK is a mitochondrial membrane protein involved in lipid and glycerolipid metabolism. Additionally we are shipping Acylglycerol Kinase Antibodies (34) and Acylglycerol Kinase Kits (4) and many more products for this protein.
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The dual function of AGK as lipid kinase and constituent of the TIM22 (show TIMM22 Proteins) complex reveals that disturbances in both phospholipid metabolism and mitochondrial protein (show COX6B2 Proteins) biogenesis contribute to the pathogenesis of Sengers syndrome.
Identify AGK as a bona fide subunit of TIM22 (show TIMM22 Proteins) providing an exciting and unexpected link between mitochondrial protein (show COX6B2 Proteins) import and Sengers syndrome.
Acylglycerol kinase functions as an oncogene (show RAB1A Proteins) and an unfavorable prognostic marker for human gliomas.
We showed that AGK was over-expressed in cervical cancer cell lines and clinical tissues, and over-expression of AGK was associated with poor survival outcomes of early-stage CSCC (show CYP11A1 Proteins) patients. AGK can be used as an independent prognostic marker for early-stage CSCC (show CYP11A1 Proteins).
Data suggest that acylglycerol kinase (AGK) has potential as a prognostic factor for overall survival in nasopharyngeal carcinoma (NPC (show NPC1 Proteins)).
AGK promotes the proliferation and cell cycle progression of oral squamous cell carcinoma.
miR (show MLXIP Proteins)-194 could reduce the phosphoinositide 3-kinase (PI3K (show PIK3CA Proteins))/AKT (show AKT1 Proteins)/FoxO3a (show FOXO3 Proteins) signaling pathway by suppressing acylglycerol kinase (AGK) directly.
findings provide new evidence that AGK plays an important role in promoting angiogenesis and providing resistance to apoptosis in hepatocellular carcinoma
compare our findings to those in 21 previously reported AGK mutation-positive Sengers patients, confirming that Sengers syndrome is a clinically recognisable disorder of mitochondrial energy metabolism
AGK promotes cell proliferation and tumorigenicity in breast cancer via suppression of the FOXO1 (show FOXO1 Proteins).
The protein encoded by this gene is a mitochondrial membrane protein involved in lipid and glycerolipid metabolism. The encoded protein is a lipid kinase that catalyzes the formation of phosphatidic and lysophosphatidic acids. Defects in this gene have been associated with mitochondrial DNA depletion syndrome 10.
, acylglycerol kinase, mitochondrial-like
, acylglycerol kinase, mitochondrial
, multi-substrate lipid kinase
, multiple substrate lipid kinase