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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 (170) and Apolipoprotein M Kits (36) and many more products for this protein.
Showing 10 out of 30 products:
Human Apolipoprotein M Protein expressed in Wheat germ - ABIN1345395
Skupien, Kepka, Gorczynska-Kosiorz, Gebska, Klupa, Wanic, Nowak, Borowiec, Sieradzki, Malecki: Evaluation of Apolipoprotein M Serum Concentration as a Biomarker of HNF-1alpha MODY. in The review of diabetic studies : RDS 2008
Show all 4 references for ABIN1345395
Human Apolipoprotein M Protein expressed in Escherichia coli (E. coli) - ABIN667777
Jiang, Zhang, Wu, Qin, Luo, Deng, Lu, Xu, Li, Ji, Xu: Increased plasma apoM levels in the patients suffered from hepatocellular carcinoma and other chronic liver diseases. in Lipids in health and disease 2008
Show all 2 references for ABIN667777
Plasma apoM concentrations are higher in patients with hyperlipidaemia than in healthy controls. Low plasma apoM levels in patients with T2DM are likely caused by diabetes but are not induced by hyperlipidaemia.
The polymorphism C-724del in the promoter region of the apoM gene could confer the risk of T2DM among eastern Han Chinese. Unfortunately, the lowing of plasma apoM levels of C-724del mutant allele carriers compared with the wide-type homozygotes carriers in T2DM patients was not statistically different in present study, so further researchs were needed by enlarging the sample
ApoM rs805296 polymorphism may be a risk factor for developing coronary artery disease [meta-analysis]
ApoM/HDL (show HSD11B1 Proteins)-C and apoM/apoA1 (show APOA1 Proteins) ratios could be used as indicators for identification of DN from healthy people and from T2DM patients.
ApoM may be a biomarker of coronary artery disease. ApoM-855 T-->C substitution provides binding sites for AP-2alpha (show TFAP2A Proteins) and reduces ApoM transcription activity
Data indicate significant association between the single nucleotide polymorphism (SNP rs805296) of apolipoprotein M (ApoM) and the susceptibility to ankylosing spondylitis (AS) among Chinese Han population in Lanzhou.
Serum apolipoprotein M was elevated in chronic obstructive pulmonary disease patients and increased gradually with chronic obstructive pulmonary disease severity.
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.
apoM might facilitate the maintenance of CD4 (show CD4 Proteins)(+) 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 Proteins) and ApoE (show APOE Proteins) have roles in the clearance of ApoM-associated sphingosine 1-phosphate
ApoM augmented insulin (show INS Proteins) secretion by maintaining the S1P (show S1PR1 Proteins) 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 Proteins).
Results show that apoM, by delivering S1P (show S1PR1 Proteins) to the S1P (show S1PR1 Proteins)(1) receptor on endothelial cells, is a vasculoprotective constituent of HDL (show APOA5 Proteins).
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 Proteins) in normal mice but also with the pathologically increased lipoprotein fraction in genetically modified mice; decreased apoM levels in apoA-I (show APOA1 Proteins)-deficient mice suggest a connection between apoM and apoA-I (show APOA1 Proteins) 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