Browse our APOE (APOE) ELISA Kits

Full name:
Apolipoprotein E ELISA Kits (APOE)
On www.antibodies-online.com are 115 Apolipoprotein E (APOE) ELISA Kits from 22 different suppliers available. Additionally we are shipping APOE Antibodies (339) and APOE Proteins (46) and many more products for this protein. A total of 513 APOE products are currently listed.
Synonyms:
AD2, AI255918, Apo-E, apoe, APOEA, apoprotein, im:7036787, LDLCQ5, LPG, wu:fb69a05, zgc:110064

Top referenced APOE ELISA Kits

  1. Human APOE ELISA Kit for Sandwich ELISA - ABIN417091 : Wu, Liu, Lei, Zhang: Comment on: Cerebrospinal fluid apolipoprotein E concentration decreases after seizure. in Seizure : the journal of the British Epilepsy Association 2010 (PubMed)
    Show all 7 references for 417091

  2. Mouse (Murine) APOE ELISA Kit for Sandwich ELISA - ABIN415472 : Escolà-Gil, Chen, Julve, Quesada, Santos, Metso, Tous, Jauhiainen, Blanco-Vaca: Hepatic lipase- and endothelial lipase-deficiency in mice promotes macrophage-to-feces RCT and HDL antioxidant properties. in Biochimica et biophysica acta 2013 (PubMed)
    Show all 2 references for 415472

More ELISA Kits for APOE Interaction Partners

Mouse (Murine) Apolipoprotein E (APOE) interaction partners

  1. treatment of APP/E4/Abca1+/- mice with liver X receptor (LXR) agonist T0 ameliorates APOE4-induced Alzheimer's disease (AD)-like pathology and therefore targeting the LXR-ABCA1-APOE regulatory axis could be effective as a potential therapeutic approach in AD patients, carriers of APOEepsilon4

  2. Adiponectin (show ADIPOQ ELISA Kits), TNF-alpha (show TNF ELISA Kits), and LOX-1 (show OLR1 ELISA Kits) exert complex regulatory effects on the coronary microvascular endothelial function in atherosclerotic ApoE knockout mice.

  3. Apoe-deficient mice and human apoE isoform knockin mice, as well as hypomorphic Apoe mice, have significantly contributed to our understanding of the role of apoE in lipoprotein metabolism. [review]

  4. beta-Sarcoglycan (show SGCB ELISA Kits) deficiency reduces atherosclerotic plaque formation in ApoE-knockout mouse model.

  5. we found that the lack of microbiota caused a significant reduction in atherosclerotic lesion formation compared with Conv ApoE(-/-) mice, which might be associated with the attenuation of lipopolysaccharide-mediated inflammatory responses. Our findings indicated that the gut (show GUSB ELISA Kits) microbiota affected both hypercholesterolemia and atherogenesis in mice

  6. this reduction in lesion formation was associated with reduced numbers of lesional SMCs but not macrophages within the transplanted Cx3cr-/- Apoe-/- aortic segment. No differences in frequencies of proliferating and apoptotic cells could be observed. These results indicate that CX3CR1 (show CX3CR1 ELISA Kits) on resident vessel wall cells plays a key role in atherosclerotic plaque formation in transplanted aortic grafts

  7. Specific inhibition of the NLRP3 (show NLRP3 ELISA Kits) inflammasome using MCC950 can be a promising therapeutic approach to inhibit atherosclerotic lesion development in ApoE deficient mice.

  8. catK (show CTSK ELISA Kits) deficiency almost completely blunted the increased vascular remodeling response of apoE-/- mice to flow cessation, possibly by correcting hyperlipidemia-associated pro-inflammatory effects on the peripheral immune response

  9. High fat intake inhibits the compensatory mechanisms of neuroinflammation and neurogenesis in aged female ApoE4 and ApoE-/- mice.

  10. The levels of EZH2 (show EZH2 ELISA Kits) and H3K27me3 were increased in the aorta of ApoE-/- mice fed a high-methionine diet for 16 weeks, whereas miR (show MLXIP ELISA Kits)-92a expression was decreased.

Human Apolipoprotein E (APOE) interaction partners

  1. the identification of the e4 allele of Apolipoprotein E as a strong genetic risk factor for both early-onset and late-onset Alzheimer disease (AD) , and evolved to the more recent detection of at least 21 additional genetic risk loci for the genetically complex form of AD emerging from genome-wide association studies

  2. APOE-epsilon2 allele was more frequent in ALS patients than in controls.

  3. Study analyzed 595 older adults without dementia classified cross-sectionally as Abeta (show APP ELISA Kits)- and Abeta (show APP ELISA Kits)+ using longitudinal florbetapir positron emission tomography. APOE epsilon4 carriage and older age were predictors of longitudinal Abeta (show APP ELISA Kits) accumulation within the Abeta (show APP ELISA Kits)- group but not the Abeta (show APP ELISA Kits)+ group. APOE epsilon2 carriage was protective against longitudinal Abeta (show APP ELISA Kits) accumulation within the Abeta (show APP ELISA Kits)- group.

  4. Meta-analysis suggested that there is no association between APOE polymorphism and subarachnoid hemorrhage risk for overall population. Increased risk of SAH (show ACSM3 ELISA Kits) was found in Asian subjects when epsilon4 allele compared with epsilon3 allele.

  5. Here, we have shown that genetic restoration of plasma ApoE to wild-type levels normalizes plasma lipids in ApoE KO mice. While this does not rescue synaptic loss, it does completely restore learning and memory in the mice, suggesting that both CNS and plasma ApoE are independent parameters that affect brain health.

  6. the results of current study found a significant gene- gene interaction between rs405509 of APOE gene polymorphism and rs1805192 of PPARG (show PPARG ELISA Kits) polymorphism associated with increased Late-Onset Alzheimer's Disease risk

  7. ApoE epsilon4 allele seems to be risk factor for major adverse cardiovascular events, and in particular for total peripheral revascularization in patients with advanced atherosclerotic vascular disease.

  8. Data suggest that the redox status of serum apoE might be related to the synthesis of HDL (show HSD11B1 ELISA Kits); the cysteine-thiol residue of reduced-apoE is in a naive state, while that of non-reduced-apoE is in a reversibly or irreversibly oxidized state. Data suggest that apoE homodimer and apoE-AII (show NLRP3 ELISA Kits) complex are typical reversibly oxidized forms of apoE. (apoE-AII (show NLRP3 ELISA Kits) complex = a complex of apolipoprotein E and apolipoprotein A-II (show APOA2 ELISA Kits))

  9. carriers of the ApoE varepsilon4 polymorphism genotype show demonstrable improvement in VA after treatment with ranibizumab in exudative AMD (show AMD1 ELISA Kits).

  10. Findings do not provide significant support for presenilin 1 (PSEN1 (show PSEN1 ELISA Kits)) E318G as a risk factor for Alzheimer's disease (AD) in apolipoprotein E4 (APOEepsilon4) carriers.

Rabbit Apolipoprotein E (APOE) interaction partners

  1. 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.

  2. The molar ratio ApoE/ApoA-I (show APOA1 ELISA Kits) 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.

  3. ApoE mimetic peptide reduces plasma lipid hydroperoxide content with a concomitant increase in HDL (show HSD11B1 ELISA Kits) paraoxonase activity

  4. 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.

Pig (Porcine) Apolipoprotein E (APOE) interaction partners

  1. These data suggest that the -155T>A mutation in the promoter region of the porcine APOE gene is an important functional variant

Cow (Bovine) Apolipoprotein E (APOE) interaction partners

  1. Nonesterified fatty acids significantly inhibit the expression of ApoB100 (show APOB ELISA Kits), ApoE, MTP (show MTTP ELISA Kits), and LDLR (show LDLR ELISA Kits), thereby decreasing the synthesis and assembly of VLDL and inducing TG accumulation in bovine hepatocytes.

  2. Bovine apoE contents in triglyceride-rich lipoproteins are modulated by nutritional treatment and closely associated with triglyceride-rich lipoprotein metabolism

  3. apoE-containing particles, which increased during the lactating stage, were not associated with HDL (show HSD11B1 ELISA Kits) particles, and lipid-free forms were included in cow plasma

  4. after calving the apolipoprotein B(100 (show APOB ELISA Kits)) mRNA synthesis was lower, whereas microsomal triglyceride transfer protein (MTP (show MTTP ELISA Kits)) and apolipoprotein E messenger RNA abundance were higher in the liver

Chimpanzee Apolipoprotein E (APOE) interaction partners

  1. 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.

  2. ApoE evolution and very likely the evolution of other apolipoproteins are influenced by feeding environment and diet of humans, chimpanzees and various other species.

Rhesus Monkey Apolipoprotein E (APOE) interaction partners

  1. In the hippocampus APOE protein levels were higher in good spatial performers than poor spatial performers animals

  2. 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

  3. There was significantly more apoE immunoreactivity in the prefrontal cortex and hippocampus of aged animals compared to adult or middle-aged animals.

APOE Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with APOE

  • apolipoprotein E (apoe) Elisa Kit
  • apolipoprotein Ea (apoea) Elisa Kit
  • apolipoprotein E (Apoe) Elisa Kit
  • apolipoprotein E (APOE) Elisa Kit
  • AD2 Elisa Kit
  • AI255918 Elisa Kit
  • Apo-E Elisa Kit
  • apoe Elisa Kit
  • APOEA Elisa Kit
  • apoprotein Elisa Kit
  • im:7036787 Elisa Kit
  • LDLCQ5 Elisa Kit
  • LPG Elisa Kit
  • wu:fb69a05 Elisa Kit
  • zgc:110064 Elisa Kit

Protein level used designations for Apolipoprotein E (APOE) ELISA Kits

apolipoprotein E , ApoE-1 , apo-E , apolipoprotein E3

GENE ID SPECIES
394678 Xenopus (Silurana) tropicalis
553587 Danio rerio
100136023 Oncorhynchus mykiss
100380959 Xenopus laevis
11816 Mus musculus
348 Homo sapiens
100009337 Oryctolagus cuniculus
25728 Rattus norvegicus
397576 Sus scrofa
100731633 Cavia porcellus
281004 Bos taurus
476438 Canis lupus familiaris
449586 Pan troglodytes
714623 Macaca mulatta
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