Abcam, ab224237, Anti-LSR antibody

Size: 100µL
Rabbit Polyclonal LSR antibody. Suitable for IHC-P, WB, ICC/IF and reacts with Human samples. Cited in 1 publication. Immunogen corresponding to Recombinant Fragment Protein within Human LSR aa 400-550.
Key facts
Host species:Rabbit,
Clonality:Polyclonal,
Isotype:IgG,
Carrier free:No,
Reacts with:Human,
Applications:IHC-P, WB, ICC/IFSee reactivity dataSee the reactivity data table below for information on validated species and application combinations.,
Immunogen:Recombinant Fragment Protein within Human LSR aa 400-550. The exact immunogen used to generate this antibody is proprietary information.Q86X29

Properties and Storage Information:
Form-Liquid, Purification technique-Affinity purification Immunogen, Storage buffer-pH: 7.2 Preservative: 0.02% Sodium azide Constituents: PBS, 40% Glycerol (glycerin, glycerine), Shipped at conditions-Blue Ice, Appropriate short-term storage duration-1-2 weeks, Appropriate short-term storage conditions-+4°C, Appropriate long-term storage conditions--20°C, Aliquoting information-Upon delivery aliquot, Storage information-Avoid freeze / thaw cycle

Supplementary Information:
This supplementary information is collated from multiple sources and compiled automatically.
The LSR protein also known as Lipolysis Stimulated Lipoprotein Receptor functions mechanically as a component of the plasma membrane where it assists in lipid metabolism. It has a mass of approximately 68 kDa and plays an important role in endocytosis and binding of apolipoproteins. LSR is expressed significantly in liver and intestinal tissues. Researchers often study it for its involvement in lipid management in the human body.
Biological function summary
LSR interacts with other proteins to form a multimeric complex that regulates lipid processing. Its presence is essential for maintaining lipid homeostasis by binding chylomicrons and cholesterol-rich lipoproteins. The LSR complex plays a significant role in managing body lipid levels and maintaining cellular health. These processes contribute to the efficient transport and clearance of dietary fats which are essential functions in metabolic regulation.
Pathways
The activity of the LSR protein is integral to the lipid metabolism and cholesterol homeostasis pathways. Within these pathways LSR collaborates with proteins like APOB and APOE to facilitate lipid uptake and processing. It functions by enabling the clearance of chylomicron remnants and very low-density lipoprotein particles from the bloodstream maintaining lipid balance and preventing disorders related to lipid accumulation.
The dysfunction or altered expression of LSR can associate with hyperlipidemia and atherosclerosis. These conditions result from impaired lipid uptake and clearance leading to elevated blood lipid levels. LSR's interaction with apolipoproteins such as APOB links its activities to the metabolic disturbances observed in these diseases. Understanding LSR's role in lipid mechanisms provides potential avenues for therapeutic interventions targeting lipid-related disorders.