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APOB product is the main apolipoprotein of chylomicrons and low density lipoproteins. Additionally we are shipping and many more products for this protein.
Showing 10 out of 20 products:
Mouse (Murine) APOB ELISA Kit for Sandwich ELISA - ABIN832333
Hu, Hu, Zhao, Li, Ma, Wu, Lu, Qiu, Sha, Wang, Gao, Zheng, Wang: An agomir of miR-144-3p accelerates plaque formation through impairing reverse cholesterol transport and promoting pro-inflammatory cytokine production. in PLoS ONE 2014
Human APOB ELISA Kit - ABIN2345039
Sukhanov, Snarski, Vaughn, Lobelle-Rich, Kim, Higashi, Shai, Delafontaine: Insulin-like growth factor I reduces lipid oxidation and foam cell formation via downregulation of 12/15-lipoxygenase. in Atherosclerosis 2015
C7673T polymorphism in apoB gene is significantly associated with increased ischemic stroke risk in the Chinese population.
Apo (show C9orf3 ELISA Kits)-B correlation with both LDL-C and non-HDL (show HSD11B1 ELISA Kits)-C is reduced in individuals with high TG levels and in particular for those with diabetes or MetS.
Report increased intestinal cholesterol absorption and elevated serum cholesterol in families with primary hypercholesterolemia without mutations in APOB.
associations between apolipoprotein B, A1, and the B/A1 ratio and nonalcoholic fatty liver disease in both normal-weight and overweight Korean population
Data indicate that serum apolipoproteins ApoB, ApoA-1 (show APOA1 ELISA Kits) and ApoB/A-1 ratio levels are independently associated with coronary heart disease (CHD (show CHDH ELISA Kits)) risk in Korean men.
Low plasma concentration of PTX3 (show PITX3 ELISA Kits) in early pregnancy is associated with subsequent development of gestational diabetes and with an enhanced risk for CVD as estimated by an elevated apoB/apoA (show APOA ELISA Kits) ratio at 5 years postpartum.
There was no correlation found between plasma apoB levels and hyperhomocysteinemia.
Homozygosity for a rare missense mutation in the betaalpha1 domain of apoB may be the cause of both severe hypobetalipoproteinemia and intestinal lipid malabsorption.
ApoB/ApoA1 SNPs are associated with alcohol-induced alcohol-induced osteonecrosis of femoral head in the Han Chinese population.
Report changes in the concentration of sialic acid in ApoB-containing lipoproteins in liver disease.
This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. It occurs in plasma as two main isoforms, apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2180 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. Mutations in this gene or its regulatory region cause hypobetalipoproteinemia, normotriglyceridemic hypobetalipoproteinemia, and hypercholesterolemia due to ligand-defective apoB, diseases affecting plasma cholesterol and apoB levels.
, apolipoprotein B (including Ag(x) antigen)
, apolipoprotein B-100
, apolipoprotein B48
, mutant Apo B 100
, apolipoprotein B