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The protein encoded by APOM is an apolipoprotein and member of the lipocalin protein family. Additionally we are shipping Apolipoprotein M Antibodies (163) and Apolipoprotein M Proteins (27) and many more products for this protein.
Showing 10 out of 40 products:
Human Apolipoprotein M ELISA Kit for Sandwich ELISA - ABIN417454
Huang, Liu, Jiang, Sun, Zhang, Liu, Xu: Apolipoprotein m (APOM) levels and APOM rs805297 G/T polymorphism are associated with increased risk of rheumatoid arthritis. in Joint, bone, spine : revue du rhumatisme 2014
Show all 2 references for ABIN417454
Mouse (Murine) Apolipoprotein M ELISA Kit for Sandwich ELISA - ABIN810844
Kurano, Tsukamoto, Hara, Ohkawa, Ikeda, Yatomi: LDL Receptor and ApoE are Involved in the Clearance of ApoM-associated Sphingosine 1-phosphate. in The Journal of biological chemistry 2014
ApoM is excreted in the urine of children after cardiac surgery in children with acute kidney injury
Hyperglycemia-induced downregulation of apolipoprotein M expression is not via the hexosamine pathway.
ApoM is highly expressed in renal proximal tubule cells and is usually reabsorbed by giantin-associated proteins in a process, which is also affected in kidney disease.
our findings present supportive evidence that ApoM is a regulator of human LRH-1 (show NR5A2 ELISA Kits) transcription, and further reveal the importance of ApoM as a critical regulator of bile acids metabolism
-724 I/D polymorphism decreases the apoM promoter activity, down-regulates the apoM protein expression level, and increases the risk of myocardial infarction
these findings demonstrated that apoM suppressed TNF-alpha (show TNF ELISA Kits)-induced expression of ICAM-1 (show ICAM1 ELISA Kits) and VCAM-1 (show VCAM1 ELISA Kits) through inhibiting the activity of NF-kappaB (show NFKB1 ELISA Kits).
role of apoM in lipid metabolism and cardiometabolic diseases.(48-55)
ApoM levels differ according to country of birth and are associated with IR and T2DM only in native-born Swedes, not Iraqis living in Sweden.
Binary logistic regression analysis suggested that both apoM and apoAI mRNA may considered as independent risk factors for fetal macrosomia
ApoM overexpression may have a potential role in improving insulin (show INS ELISA Kits) resistance in vivo and modulating apoM expression might be a future therapeutic strategy against insulin (show INS ELISA Kits) resistance in type 2 diabetes.
apoM might facilitate the maintenance of CD4 (show CD4 ELISA Kits)(+) T-lymphocytes or could modify the T-lymphocytes subgroups in murine spleen
Upon immune stimulation, Apom(-/-) mice developed more severe experimental autoimmune encephalomyelitis, characterized by increased lymphocytes in the central nervous system and breakdown of the blood-brain barrier
LDL receptor (show LDLR ELISA Kits) and ApoE (show APOE ELISA Kits) have roles in the clearance of ApoM-associated sphingosine 1-phosphate
ApoM augmented insulin (show INS ELISA Kits) secretion by maintaining the S1P (show S1PR1 ELISA Kits) concentration under both in vivo and in vitro conditions.
The present data indicate that the plasma apo-M levels modulate the ability of plasma to mobilize cellular cholesterol, whereas apo-M has no major effect on the excretion of cholesterol into feces.
ApoM can bind oxidized phospholipids, increasing the antioxidant effect of HDL (show HSD11B1 ELISA Kits).
Results show that apoM, by delivering S1P (show S1PR1 ELISA Kits) to the S1P (show S1PR1 ELISA Kits)(1) receptor on endothelial cells, is a vasculoprotective constituent of HDL (show APOA5 ELISA Kits).
After refolding from inclusion bodies, the crystal structure of apoM (reported here at 2.5 A resolution) displays a novel yet unprecedented seven-stranded beta-barrel structure.
apoM mainly associates with HDL (show HSD11B1 ELISA Kits) in normal mice but also with the pathologically increased lipoprotein fraction in genetically modified mice; decreased apoM levels in apoA-I (show APOA1 ELISA Kits)-deficient mice suggest a connection between apoM and apoA-I (show APOA1 ELISA Kits) metabolism.
ApoM transcripts were detectable in mouse embryos from day 7.5 to day 18.5
The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene.
, NG20-like protein
, alternative name: G3a, NG20
, protein G3a
, protein Px