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anti-Mouse (Murine) APOE Antikörper:
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Human Monoclonal APOE Primary Antibody für CyTOF, ELISA - ABIN258785
Wahrle, Jiang, Parsadanian, Hartman, Bales, Paul, Holtzman: Deletion of Abca1 increases Abeta deposition in the PDAPP transgenic mouse model of Alzheimer disease. in The Journal of biological chemistry 2005
Show all 10 Pubmed References
Human Polyclonal APOE Primary Antibody für IHC, WB - ABIN2774066
Ho, Niti, Yap, Kua, Ng: Metabolic syndrome and cognitive decline in chinese older adults: results from the singapore longitudinal ageing studies. in The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry 2008
Show all 4 Pubmed References
Human Monoclonal APOE Primary Antibody für IHC (fro), IHC (p) - ABIN536226
Zunarelli, Nicoll, Migaldi, Trentini: Apolipoprotein E polymorphism and breast carcinoma: correlation with cell proliferation indices and clinical outcome. in Breast cancer research and treatment 2001
Show all 3 Pubmed References
Human Polyclonal APOE Primary Antibody für IHC (p), ELISA - ABIN1997537
Li, Jiang, Qu, Yao, Cai, Chen, Peng: Hepatocyte nuclear factor 4? and downstream secreted phospholipase A2 GXIIB regulate production of infectious hepatitis C virus. in Journal of virology 2013
Show all 2 Pubmed References
Human Monoclonal APOE Primary Antibody für FACS, IHC - ABIN968962
Karpouzis, Caridha, Tripsianis, Michailidis, Martinis, Veletza: Apolipoprotein E gene polymorphism in psoriasis. in Archives of dermatological research 2009
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Human Polyclonal APOE Primary Antibody für IHC (p), WB - ABIN391849
Benga, Krieger, Dimitrova, Zeisel, Parnot, Lupberger, Hildt, Luo, McLauchlan, Baumert, Schuster: Apolipoprotein E interacts with hepatitis C virus nonstructural protein 5A and determines assembly of infectious particles. in Hepatology (Baltimore, Md.) 2009
Mouse (Murine) Polyclonal APOE Primary Antibody für ID, RID - ABIN151509
Terwel, Steffensen, Verghese, Kummer, Gustafsson, Holtzman, Heneka: Critical role of astroglial apolipoprotein E and liver X receptor-α expression for microglial Aβ phagocytosis. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Human Polyclonal APOE Primary Antibody für IHC (p), IP - ABIN152926
Atkinson, Blumenstein, Black, Wu, Kasabov, Taylor, Cooper, North: An altered pattern of circulating apolipoprotein E3 isoforms is implicated in preeclampsia. in Journal of lipid research 2008
Mouse (Murine) Polyclonal APOE Primary Antibody für IF (p), IHC (p) - ABIN725750
Chiu, Chan, Yang, Liu, Chiang: Supplementation of Chitosan Alleviates High-Fat Diet-Enhanced Lipogenesis in Rats via Adenosine Monophosphate (AMP)-Activated Protein Kinase Activation and Inhibition of Lipogenesis-Associated Genes. in Journal of agricultural and food chemistry 2015
Human Monoclonal APOE Primary Antibody für FACS, IHC - ABIN965577
Zintzaras, Kitsios, Triposkiadis, Lau, Raman: APOE gene polymorphisms and response to statin therapy. in The pharmacogenomics journal 2009
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Deletion of apolipoprotein E in astrocytes ameliorates the spatial learning and memory deficits in Alzheimer's disease by inhibiting TGF-beta (zeige TGFB1 Antikörper)/Smad2 (zeige SMAD2 Antikörper)/STAT3 (zeige STAT3 Antikörper) signaling.
choroid plexus/CSF (zeige CSF2 Antikörper) provides an additional source of apoE and the glymphatic fluid transporting system delivers it to brain via the periarterial space
Longxuetongluo capsule inhibits atherosclerosis progression in high-fat diet-induced ApoE(-/-) mice by improving endothelial dysfunction via MAPK (zeige MAPK1 Antikörper)/IKK (zeige CHUK Antikörper)/IkappaB/NF-kappaB (zeige NFKB1 Antikörper) signaling pathway.
Major orthopedic surgery in ApoE-/- mice triggers a systemic inflammatory response. Atherosclerotic plaque area is enlarged after surgery mainly due to an increase of the necrotic core.
Saffron (Crocus sativus) protects against myocardial ischemia-reperfusion injury in Wild Type and ApoE((-/-)) mice via Nrf2 (zeige NFE2L2 Antikörper) pathway.
Zinc supplementation has a therapeutic effect on the advanced atherosclerosis of ApoE gene-deleted mice, which can significantly improve the efficacy of irbesartan.
Decreased Hexim-1 (zeige HEXIM1 Antikörper) expression does not alter cholesterol metabolism in ApoE null background after high fat diet. However, it promotes stable atherosclerotic plaque and decreased steatosis by promoting the anti-inflammatory TGFbeta (zeige TGFB1 Antikörper) pathway and blocking the expression of the inducible and pro-inflammatory expression of SOCS3 (zeige SOCS3 Antikörper) respectively.
DPP-4 (zeige DPP4 Antikörper) inhibitor teneligliptin inhibited atherogenesis in ApoE knockout mice, at least partially, through attenuation of the inflammatory phenotype of perivascular adipose tissue.
Loss of ApoE potentiates a semi-chronic inflammatory arthritis.
apoE4 interacts wiith insulin receptor (zeige INSR Antikörper) and impairs its trafficking by trapping it in the endosomes, leading to impaired insulin (zeige INS Antikörper) signaling and insulin (zeige INS Antikörper)-stimulated mitochondrial respiration and glycolysis.
In this study, we found no significant association between allele and genotype frequencies of APOE; the intronic SNP rs2165241 and the non-synonymous SNP rs3825942 in exon 1 of LOXL1 (zeige LOXL1 Antikörper) are significantly associated with pseudoexfoliation syndrome and exfoliation glaucoma in the Turkish population.
APOE epsilon4 allele is neither a risk factor for rapid eye movement sleep behavior disorder(RBD (zeige CACNA1D Antikörper)) nor it is associated with conversion from RBD (zeige CACNA1D Antikörper) to dementia with Lewy bodies or other synucleinopathies.
APOE genotype presents a systematic array of potential associations with cognitive performance
APOE epsilon4 genotype is the major driver of accumulation of white matter hyperintensities volume.
APOE epsilon4 allele increases the risk for sporadic Alzheimer's disease and modifies brain activation patterns of numerous cognitive domains.
indicates that measurable apolipoprotein E-related brain atrophy does not occur in early adulthood and midlife
Self-reported sleep duration, napping, and trouble falling/staying asleep differ by APOE genotype; studies are needed to examine whether APOE promotes AD by degrading sleep and to clarify the role of race in these associations
Study provides support for the argument that Apolipoprotein E (APOE varepsilon4+) and catechol-O-methyl transferase Met/Met genotypes can be used as predictors of faster cognitive decline in Parkinson's disease.
both apolipoprotein E and Abeta1-42 abundance can differ depending upon the type of CJD (zeige PRNP Antikörper).
report association of APOE and TOMM40 (zeige TOMM40 Antikörper) with behavioural variant frontotemporal dementia, and ARHGAP35 (zeige GRLF1 Antikörper) and SERPINA1 (zeige SERPINA1 Antikörper) with progressive non-fluent aphasia.
we report the efficient creation of an APOE knockout rabbit by using zinc finger nucleases. The knockout rabbits had drastically elevated cholesterol and moderately increased triglyceride levels, mimicking symptoms in human heart disease.
The molar ratio ApoE/ApoA-I (zeige APOA1 Antikörper) is negatively correlated with the enzyme activity, and positively correlated with increases in the intima-media thickness of common carotid wall and cardiac dysfunction signs.
ApoE mimetic peptide reduces plasma lipid hydroperoxide content with a concomitant increase in HDL (zeige HSD11B1 Antikörper) paraoxonase activity
The identification of disulphide-linked apoE dimers in cortical and hippocampal tissues represents a distinct structural difference between the apoE3 and apoE4 isoforms that may have functional consequences.
These data suggest that the -155T>A mutation in the promoter region of the porcine APOE gene is an important functional variant
Nonesterified fatty acids significantly inhibit the expression of ApoB100 (zeige APOB Antikörper), ApoE, MTP (zeige MTTP Antikörper), and LDLR (zeige LDLR Antikörper), thereby decreasing the synthesis and assembly of VLDL and inducing TG accumulation in bovine hepatocytes.
Bovine apoE contents in triglyceride-rich lipoproteins are modulated by nutritional treatment and closely associated with triglyceride-rich lipoprotein metabolism
apoE-containing particles, which increased during the lactating stage, were not associated with HDL (zeige HSD11B1 Antikörper) particles, and lipid-free forms were included in cow plasma
after calving the apolipoprotein B(100 (zeige APOB Antikörper)) mRNA synthesis was lower, whereas microsomal triglyceride transfer protein (MTP (zeige MTTP Antikörper)) and apolipoprotein E messenger RNA abundance were higher in the liver
The study found no coding variation within and between chimpanzee populations, suggesting that the maintenance of functionally diverse APOE polymorphisms is a unique feature of human evolution.
ApoE evolution and very likely the evolution of other apolipoproteins are influenced by feeding environment and diet of humans, chimpanzees and various other species.
In the hippocampus APOE protein levels were higher in good spatial performers than poor spatial performers animals
Allele frequencies of the ApoE gene found show that allele epsilon3 has one of the highest frequencies and epsilon4 allele one of the lowest compared to other population groups in the world
There was significantly more apoE immunoreactivity in the prefrontal cortex and hippocampus of aged animals compared to adult or middle-aged animals.
Chylomicron remnants and very low density lipoprotein (VLDL) remnants are rapidly removed from the circulation by receptor-mediated endocytosis in the liver. Apolipoprotein E, a main apoprotein of the chylomicron, binds to a specific receptor on liver cells and peripheral cells. ApoE is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. The APOE gene is mapped to chromosome 19 in a cluster with APOC1 and APOC2. Defects in apolipoprotein E result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants.
, apolipoprotein E3