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Human Polyclonal APOA4 Primary Antibody for IHC, IHC (p) - ABIN4281185
Levin, Wang, Schwarz, Koethe, Leweke, Bahn: Global proteomic profiling reveals altered proteomic signature in schizophrenia serum. in Molecular psychiatry 2010
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Human Monoclonal APOA4 Primary Antibody for ELISA, WB - ABIN968958
Peignon, Thenet, Schreider, Fouquet, Ribeiro, Dussaulx, Chambaz, Cardot, Pinçon-Raymond, Le Beyec: E-cadherin-dependent transcriptional control of apolipoprotein A-IV gene expression in intestinal epithelial cells: a role for the hepatic nuclear factor 4. in The Journal of biological chemistry 2006
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Human Monoclonal APOA4 Primary Antibody for ELISA, WB - ABIN968959
Chien, Chen, Hsu, Su, Chang, Lee, Lee: Genetic association study of APOA1/C3/A4/A5 gene cluster and haplotypes on triglyceride and HDL cholesterol in a community-based population. in Clinica chimica acta; international journal of clinical chemistry 2007
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Human Polyclonal APOA4 Primary Antibody for WB - ABIN2785651
Penco, Buscema, Patrosso, Marocchi, Grossi: New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background. in BMC bioinformatics 2008
Human Polyclonal APOA4 Primary Antibody for IHC, IHC (p) - ABIN4281184
Kato, Nicholson, Neiman, Rantalainen, Holmes, Barrett, Uhlén, Nilsson, Spector, Schwenk: Variance decomposition of protein profiles from antibody arrays using a longitudinal twin model. in Proteome science 2011
Mouse (Murine) Polyclonal APOA4 Primary Antibody for ELISA, IHC - ABIN449527
Orsó, Moehle, Boettcher, Szakszon, Werner, Langmann, Liebisch, Buechler, Ritter, Kronenberg, Dieplinger, Bornstein, Stremmel, Schmitz: The satiety factor apolipoprotein A-IV modulates intestinal epithelial permeability through its interaction with alpha-catenin: implications for inflammatory bowel diseases. in Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2007
Human Polyclonal APOA4 Primary Antibody for IHC (p), IHC - ABIN188729
Spaulding, Saijo, Turnage, Alexander, Aw, Kalogeris: Apolipoprotein A-IV attenuates oxidant-induced apoptosis in mitotic competent, undifferentiated cells by modulating intracellular glutathione redox balance. in American journal of physiology. Cell physiology 2005
Human Polyclonal APOA4 Primary Antibody for IHC (p), WB - ABIN513413
Huang, Wu, Tseng, Chen, Hsieh, Chen: Increased prothrombin, apolipoprotein A-IV, and haptoglobin in the cerebrospinal fluid of patients with Huntington's disease. in PLoS ONE 2011
The genotype-risk associations were examined between APOA4 (rs5095, rs675, rs5110) and obesity-related phenotypes and other comorbidities in Sucre, Venezuela. There was a higher average waist-hip ratio among rs5095 homozygotes and for conicity index among homozygotes for rs5110.
Apolipoprotein L1 (显示 APOL1 抗体) and apolipoprotein A-IV and their association with kidney function
APOA-IV glycation is associated with coronary artery disease severity in patients with Type 2 Diabetes Mellitus.
These findings indicate that LZIP (显示 CREB3 抗体) is a novel modulator of APOA4 expression and hepatic lipid metabolism.
Study discovered novel and independent associations of prediabetes and related traits with MASP1 (显示 MASP1 抗体), and some evidence for associations with THBS1 (显示 THBS1 抗体), GPLD1 (显示 GPLD1 抗体) and ApoA-IV, suggesting a role for these proteins in the pathophysiology of type 2 diabetes.
Analyses of SNP-scores indicate potential causal effects of kidney function and by lesser extent triglycerides on apoA-IV concentrations.
Low levels of APOA1 (显示 APOA1 抗体), APOC3 (显示 APOC3 抗体), and APOA4 are associated with risk of Alzheimer disease.
Single nucleotide polymorphisms (Rs7396835) of APOA4 protein did not increase the risk of CHD (显示 CHDH 抗体) in the Chinese population.
ApoA-IV colocalizes with NR4A1 (显示 NR4A1 抗体), which suppresses G6Pase (显示 G6PC 抗体) and PEPCK (显示 PEPCK 抗体) gene expression at the transcriptional level, reducing hepatic glucose output and lowering blood glucose.
the present findings reveal that High-altitude polycythemia -induced gastric mucosal lesion inspires the protection responses by up-regulating APOA4 and APOC3 (显示 APOC3 抗体), and down-regulating GIF (显示 GIF 抗体).
MTTP (显示 MTTP 抗体) is regulated by apo A-IV in manner to promote increased packaging of triglyceride into chylomicron core, which may be important in neonatal fat absorption.
down-regulation of apolipoprotein A-I (显示 APOA1 抗体) and A-IV messages in the liver may be mediated by interleukin 6 (显示 IL6 抗体) and tumor necrosis factor-alpha (显示 TNF 抗体)
Hepatocyte nuclear factor 4 alpha (HNF-4 alpha (显示 HNF4A 抗体))induces apoliprotein IV gene in response to dietary lipids in the intestine.
APOA4 genes with SNPs
Upregulation of the intestinal apolipoprotein APOA-IV in horses with chronic laminitis was confirmed by western blot.[APOA-IV]
This study uncovers an anti-sense lncRNA (APOA4-AS), which is co-expressed with APOA4, and concordantly and specifically regulates APOA4 expression both in vitro and in vivo with the involvement of HuR (显示 ELAVL1 抗体).
Our findings may throw light on the function of ApoA4 in inflammatory responses and acute-phase reactions, as well as the development of SERPINA3 (显示 SERPINA3 抗体) relative diseases.
Very Low Density Lipoprotein (VLDL) assembly and CREBH (显示 CREB3L3 抗体) activation play key roles in the response to hepatic steatosis by up-regulating apoA-IV and promoting assembly and secretion of larger, more triglyceride - enriched VLDL particles.
It was suggested that increased ileal GPR119 (显示 GPR119 抗体) is a potential mechanism by which GLP-1 (显示 GCG 抗体) secretion is enhanced in apoA-IV-/- mice.
these data suggest that apoA-IV is not necessary for the metabolic improvements shown with VSG, but also suggest an interesting role for apoA-IV in regulating macronutrient preference and hepatic triglyceride levels.
These results reveal ApoA-IV as a novel follicle-associated epithelium-specific marker especially in the upper small intestine of adult mice.
transcriptional regulation of apolipoprotein A-IV by the transcription factor CREBH (显示 CREB3L3 抗体)
apoA-IV inhibits hepatic gluconeogenesis by decreasing Glc-6-Pase (显示 G6PC 抗体) and PEPCK (显示 PEPCK 抗体) gene expression through NR1D1 (显示 NR1D1 抗体).
Hepatic steatosis in mice induces hepatic apoA-IV expression, which in turn promotes lipoprotein particle expansion and reduces hepatic lipid burden without increasing the number of secreted atherogenic apoB (显示 APOB 抗体)-containing lipoprotein particles.
Data indicate that plasma lipids, lipid absorption, and microsomal triglyceride transfer protein (MTP (显示 MTTP 抗体)), FoxO1 (显示 FOXO1 抗体), and FoxA2 (显示 FOXA2 抗体) levels are lower at night and at mealtime in apoAIV-/- mice.
Apoliprotein (apo) A-IV gene contains 3 exons separated by two introns. A sequence polymorphism has been identified in the 3'UTR of the third exon. The primary translation product is a 396-residue preprotein which after proteolytic processing is secreted its primary site of synthesis, the intestine, in association with chylomicron particles. Although its precise function is not known, apo A-IV is a potent activator of lecithin-cholesterol acyltransferase in vitro.
, apolipoprotein A4
, apolipoprotein A-IV
, apolipoprotein A-IV-like