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AB27543

Anti-Apolipoprotein E3 抗体

Anti-Apolipoprotein E3 antibody

4

(1 Review)

|

(1 Publication)

Rabbit Polyclonal Apolipoprotein E antibody. Suitable for ELISA, WB, IHC-P and reacts with Human samples. Cited in 1 publication. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human APOE.

別名を表示する

Apolipoprotein E, Apo-E, APOE

Key facts

宿主種

Rabbit

クローン性

Polyclonal

アイソタイプ

IgG

キャリアフリー

No

交差種

Human

アプリケーション

WB, ELISA, IHC-P

applications

免疫原

Recombinant Full Length Protein corresponding to Human APOE.

P02649

特異性

Ab27543 recognises Apolipoprotein EIII and cross reacts with Apolipoprotein EII and Apolipoprotein EIV.

Reactivity data

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製品の詳細

Although some customers have been successful in IHC we no longer batch test in this application.

出荷温度及び保存条件

製品の状態
Lyophilized
再構成
Reconstitute in water
精製方法
Affinity purification Immunogen
精製に関する特記事項
Ab27543 was purified by affinity chromatography employing immobilized matrix.
バッファー組成
Constituents: PBS
出荷温度
Blue Ice
短期保存期間
1-2 weeks
短期保存温度
+4°C
長期保存温度
-20°C
分注に関する情報
Upon delivery aliquot

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

Apolipoprotein E3 also known as ApoE3 or Apo E3 is an important molecule in lipid metabolism. The protein has a molecular weight of approximately 34 kDa. It is mainly expressed in the liver though significant amounts are produced by astrocytes and microglia in the central nervous system. ApoE3 is one of three major isoforms of apolipoprotein E and it plays an important role in the transport and clearance of lipids especially cholesterol by binding to lipoproteins and cellular receptors.
Biological function summary

The protein participates in lipid transport and homeostasis. ApoE3 binds to lipoprotein particles forming a complex that is essential for the proper transport of lipids in the bloodstream. This binding mechanism facilitates the uptake of lipoprotein particles by cells through receptor-mediated endocytosis. ApoE3 interacts closely with other lipid-associated proteins and receptor molecules enabling the efficient delivery of cholesterol and phospholipids to many tissues which is critical for maintaining cellular membrane integrity and other lipid-based biological functions.

Pathways

ApoE3 is an important player in the cholesterol metabolism and reverse cholesterol transport pathways. The protein interacts with LDL and HDL receptors which regulate cholesterol levels in the plasma. ApoE3's role in the hepatic clearance of chylomicrons and other lipoprotein remnants is significant for maintaining lipid balance. Additionally it cooperates with proteins like LDLR (Low-Density Lipoprotein Receptor) and LRP1 (LDL Receptor Related Protein 1) in orchestrating these pathways.

Research has shown that ApoE3 is less associated with adverse conditions than other isoforms like ApoE4. However disruptions in ApoE3 function or expression can contribute to dyslipidemia and cardiovascular diseases. In Alzheimer's disease the protein's isoforms particularly ApoE4 have varying implications but understanding ApoE3's interactions can provide insights into lipid-related pathology. ApoE3's connection with LDLR and its modulation of cholesterol levels underline its potential therapeutic role in managing such disorders.

製品プロトコール

For this product, it's our understanding that no specific protocols are required. You can visit:

ターゲットの情報

APOE is an apolipoprotein, a protein associating with lipid particles, that mainly functions in lipoprotein-mediated lipid transport between organs via the plasma and interstitial fluids (PubMed : 14754908, PubMed : 1911868, PubMed : 6860692). APOE is a core component of plasma lipoproteins and is involved in their production, conversion and clearance (PubMed : 14754908, PubMed : 1911868, PubMed : 1917954, PubMed : 23620513, PubMed : 2762297, PubMed : 6860692, PubMed : 9395455). Apolipoproteins are amphipathic molecules that interact both with lipids of the lipoprotein particle core and the aqueous environment of the plasma (PubMed : 2762297, PubMed : 6860692, PubMed : 9395455). As such, APOE associates with chylomicrons, chylomicron remnants, very low density lipoproteins (VLDL) and intermediate density lipoproteins (IDL) but shows a preferential binding to high-density lipoproteins (HDL) (PubMed : 1911868, PubMed : 6860692). It also binds a wide range of cellular receptors including the LDL receptor/LDLR, the LDL receptor-related proteins LRP1, LRP2 and LRP8 and the very low-density lipoprotein receptor/VLDLR that mediate the cellular uptake of the APOE-containing lipoprotein particles (PubMed : 12950167, PubMed : 1530612, PubMed : 1917954, PubMed : 20030366, PubMed : 20303980, PubMed : 2063194, PubMed : 2762297, PubMed : 7635945, PubMed : 7768901, PubMed : 8756331, PubMed : 8939961). Finally, APOE also has a heparin-binding activity and binds heparan-sulfate proteoglycans on the surface of cells, a property that supports the capture and the receptor-mediated uptake of APOE-containing lipoproteins by cells (PubMed : 23676495, PubMed : 7635945, PubMed : 9395455, PubMed : 9488694). A main function of APOE is to mediate lipoprotein clearance through the uptake of chylomicrons, VLDLs, and HDLs by hepatocytes (PubMed : 1911868, PubMed : 1917954, PubMed : 23676495, PubMed : 29516132, PubMed : 9395455). APOE is also involved in the biosynthesis by the liver of VLDLs as well as their uptake by peripheral tissues ensuring the delivery of triglycerides and energy storage in muscle, heart and adipose tissues (PubMed : 2762297, PubMed : 29516132). By participating in the lipoprotein-mediated distribution of lipids among tissues, APOE plays a critical role in plasma and tissues lipid homeostasis (PubMed : 1917954, PubMed : 2762297, PubMed : 29516132). APOE is also involved in two steps of reverse cholesterol transport, the HDLs-mediated transport of cholesterol from peripheral tissues to the liver, and thereby plays an important role in cholesterol homeostasis (PubMed : 14754908, PubMed : 23620513, PubMed : 9395455). First, it is functionally associated with ABCA1 in the biogenesis of HDLs in tissues (PubMed : 14754908, PubMed : 23620513). Second, it is enriched in circulating HDLs and mediates their uptake by hepatocytes (PubMed : 9395455). APOE also plays an important role in lipid transport in the central nervous system, regulating neuron survival and sprouting (PubMed : 25173806, PubMed : 8939961). APOE is also involved in innate and adaptive immune responses, controlling for instance the survival of myeloid-derived suppressor cells (By similarity). Binds to the immune cell receptor LILRB4 (PubMed : 30333625). APOE may also play a role in transcription regulation through a receptor-dependent and cholesterol-independent mechanism, that activates MAP3K12 and a non-canonical MAPK signal transduction pathway that results in enhanced AP-1-mediated transcription of APP (PubMed : 28111074).. (Microbial infection) Through its interaction with HCV envelope glycoprotein E2, participates in the attachment of HCV to HSPGs and other receptors (LDLr, VLDLr, and SR-B1) on the cell surface and to the assembly, maturation and infectivity of HCV viral particles (PubMed : 25122793, PubMed : 29695434). This interaction is probably promoted via the up-regulation of cellular autophagy by the virus (PubMed : 29695434).
See full target information APOE

文献 (1)

Recent publications for all applications. Explore the full list and refine your search

Proceedings of the National Academy of Sciences of 108:18637-42 PubMed22049339

2011

Vascular ligand-receptor mapping by direct combinatorial selection in cancer patients.

Applications

IHC-P

Species

Human

Fernanda I Staquicini,Marina Cardó-Vila,Mikhail G Kolonin,Martin Trepel,Julianna K Edwards,Diana N Nunes,Anna Sergeeva,Eleni Efstathiou,Jessica Sun,Nalvo F Almeida,Shi-Ming Tu,Gregory H Botz,Michael J Wallace,David J O'Connell,Stan Krajewski,Jeffrey E Gershenwald,Jeffrey J Molldrem,Anne L Flamm,Erkki Koivunen,Rebecca D Pentz,Emmanuel Dias-Neto,João C Setubal,Dolores J Cahill,Patricia Troncoso,Kim-Ahn Do,Christopher J Logothetis,Richard L Sidman,Renata Pasqualini,Wadih Arap
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