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APOB product is the main apolipoprotein of chylomicrons and low density lipoproteins. Zusätzlich bieten wir Ihnen APOB Kits (135) und APOB Proteine (18) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 359 products:
Human Monoclonal APOB Primary Antibody für ICC, FACS - ABIN968961
Peterson, Mack, Hall, Alsup, Alexander, Sully, Sawires, Cheung, Otto, Gresham: Apolipoprotein B Is an innate barrier against invasive Staphylococcus aureus infection. in Cell host & microbe 2008
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Guinea Pig Polyclonal APOB Primary Antibody für ID - ABIN2477467
Hazell, Arnold, Flowers, Waeg, Malle, Stocker: Presence of hypochlorite-modified proteins in human atherosclerotic lesions. in The Journal of clinical investigation 1996
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Human Monoclonal APOB Primary Antibody für FACS, IF - ABIN965573
Benn: Apolipoprotein B levels, APOB alleles, and risk of ischemic cardiovascular disease in the general population, a review. in Atherosclerosis 2009
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Human Polyclonal APOB Primary Antibody für ELISA, WB - ABIN449695
Benn, Nordestgaard, Jensen, Tybjaerg-Hansen: Polymorphisms in apolipoprotein B and risk of ischemic stroke. in The Journal of clinical endocrinology and metabolism 2007
Human Polyclonal APOB Primary Antibody für RID, WB - ABIN152417
Tsai, Hsu, Hsu, Lai, Chen, Shen, Huang, Chen, Lee, Tsai, Hsu, Wu, Huang, Shiao, Hsiao, Tsou: MicroRNA-122 plays a critical role in liver homeostasis and hepatocarcinogenesis. in The Journal of clinical investigation 2012
Human Polyclonal APOB Primary Antibody für IHC (p), IP - ABIN267960
Bakillah, Tedla, Ayoub, John, Norin, Hussain, Brown: Plasma Nitration of High-Density and Low-Density Lipoproteins in Chronic Kidney Disease Patients Receiving Kidney Transplants. in Mediators of inflammation 2015
Human Monoclonal APOB Primary Antibody für RIA, ELISA - ABIN535615
Lin, Gordon, Wetterau: Microsomal triglyceride transfer protein (MTP) regulation in HepG2 cells: insulin negatively regulates MTP gene expression. in Journal of lipid research 1995
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Human Polyclonal APOB Primary Antibody für IF (p), IHC (p) - ABIN872950
Choi, de Poot, Lee, Kim, Han, Kim, Finley, Lee: Open-gate mutants of the mammalian proteasome show enhanced ubiquitin-conjugate degradation. in Nature communications 2016
Human Polyclonal APOB Primary Antibody für IP, ELISA - ABIN2477466
Davidson, Appel, Doster, Baker, Brown: Diseases and parasites of red foxes, gray foxes, and coyotes from commercial sources selling to fox-chasing enclosures. in Journal of wildlife diseases 1993
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that apos involved in TG metabolism such as apoC2 (zeige APOC2 Antikörper), C3, E, and A4 (micromolar concentration), and apoB48 and apoA5 (zeige APOA5 Antikörper) (single-digit nanomolar concentration) can be quantified from a single digestion mixture.
These findings indicate that maternal apo (zeige C9orf3 Antikörper) B levels are significantly associated with apo (zeige C9orf3 Antikörper) B levels in their pre-school age children, adjusted for confounding variables. Furthermore, the mother-child correlations in apo (zeige C9orf3 Antikörper) B levels were independent of mother-child adiposity. Measurement of apo (zeige C9orf3 Antikörper) B levels in mothers may identify both high-risk children and mothers who may benefit from intervention.
Individuals with apoB higher than predicted by non-HDL (zeige HSD11B1 Antikörper)-C had significantly higher levels of PAI-1 (zeige SERPINE1 Antikörper), which may contribute to the increased risk of future atherothrombotic events
analysis of five likely pathogenic heterozygous rare variants that include four novel nonsense mutations in APOB (p.Gln845*, p.Gln2571*, p.Cys2933* and p.Ser3718*) and a rare variant in PCSK9 (zeige PCSK9 Antikörper) (Minor Allele Frequency <0.1%).
The impact of smoking on the levels of apolipoprotein B (APOB) was evaluated by analyzing data from NHANES for the years 2007-2012 for US adolescents aged 12-19 years and adults aged greater than or eqult to 20 years. The study found that smoking did not influence the observed levels of APOB for either adolescents or adults.
Identify LDLR (zeige LDLR Antikörper), APOB and PCSK9 (zeige PCSK9 Antikörper) novel mutations causing familial hypercholesterolemia in the central south region of China.
Rare variants of APOB or PCSK9 (zeige PCSK9 Antikörper) were identified in nine of the 22 study patients with extremely low LDL-C levels
Eicosapentaenoic acid has direct antioxidant benefits in various apoB-containing subfractions.
Association of plasma apoB with IR in obese subjects is dependent on gynoid WAT dysfunction
Serum ApoB was not significantly different between term SGA newborns and control term newborns.
enhanced VLDL TG secretion in the absence of hepatocyte ABCA1 (zeige ABCA1 Antikörper) is due to altered intracellular trafficking of apolipoprotein B (apoB), resulting in augmented TG addition to nascent VLDL.
We carried out our experiment in mice deficient in the low density lipoprotein (LDL) receptor (zeige LDLR Antikörper) and expressing only ApoB100 molecule (ApoB - LDLr (zeige LDLR Antikörper)) where the development of atherosclerosis is known to closely mimic human atherosclerosis
The effect of hypercholesterolemia induced immune response and inflammation on progression of atherosclerosis in ApoB(tm25gy) LDLr (zeige LDLR Antikörper)(tm1Her) mice, expressing only ApoB100 and deficient in the low density lipoprotein receptor (zeige LDLR Antikörper).
ApoB-containing lipoproteins contribute to augmentation of AngII-induced abdominal aortic aneurysms in male mice.
Immunization with human apolipoprotein B100 (ApoB) resulted in four-fold increased accumulation of effector T cells in ApoB-containing matrigel
PCSK9 (zeige PCSK9 Antikörper) markedly increases intestinal triglyceride-rich apoB production through mechanisms mediated in part by transcriptional effects on apoB.
Mice that produce apoB100 in the RPE (zeige RPE Antikörper) and liver secrete lipoproteins into Bruch's membrane, but not to the extent that distinct features of AMD (zeige AMD1 Antikörper) develop
The aim of this study was to characterize the ocular morphology of low-density lipoprotein receptor-deficient apolipoprotein B-100-only mice, with IGF-II overexpression.
Our data establish the role of APOB gene in severe gut (zeige GUSB Antikörper) dysmotility.
Cardiac lipotoxicity may originate from direct inhibition of myocardial ApoB lipoprotein and subsequent decreased lipid export, caused by supraphysiological levels of catecholamines.
The clinicopathological phenotype of affected Holstein cattle homozygous for the causative apolipoprotein B gene (APOB) mutation associated with cholesterol deficiency is described.
Beyond malabsorption of dietary lipids, deleterious effects of apolipoprotein B deficiency on hepatic lipid metabolism, steroid biosynthesis, and cell membrane function can be expected, which may result in unspecific symptoms of reduced fertility, growth, and health.
Cholesterol deficiency results from a 1.3kbp insertion of an endogenous retrovirus (ERV2-1-LTR_BT) into exon 5 of the APOB gene at BTA11:77,959kb. The insertion is flanked by 6bp target site duplications as described for insertions mediated by retroviral integrases.
A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle
Nonesterified fatty acids significantly inhibit the expression of ApoB100, ApoE (zeige APOE Antikörper), MTP (zeige MTTP Antikörper), and LDLR (zeige LDLR Antikörper), thereby decreasing the synthesis and assembly of VLDL and inducing TG accumulation in bovine hepatocytes.
after calving the apolipoprotein B(100) mRNA synthesis was lower, whereas microsomal triglyceride transfer protein (MTP (zeige MTTP Antikörper)) and apolipoprotein E (zeige APOE Antikörper) messenger RNA abundance were higher in the liver.
found association between genotypes for LDLR (zeige LDLR Antikörper) and APOB polymorphisms and serum lipid levels, but none of them seem to be the causal mutation but probably represent closely linked polymorphisms
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 PI
, apolipoprotein B-48
, apolipoprotein B