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NSJ Bioreagents

SKU:F50536-0.08ML

ApoE Antibody (Apolipoprotein E)

ApoE Antibody (Apolipoprotein E)

Regular price $205.00 USD
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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.

Specifications

Family Primary antibody
Formulation In 1X PBS, pH 7.4, with 0.09% sodium azide
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit Ig
Species Reactivity Human
Predicted Species Reactivity Primate, Rabbit
Application IHC, WB, ELISA
Application Details Western blot: 1:1000,IHC (Paraffin): 1:10-1:50
Application Note Titration of the ApoE antibody may be required due to differences in protocols and secondary/substrate sensitivity.
Localization Cytoplasmic, membranous
Immunogen A portion of amino acids 263-292 from the human protein was used as the immunogen for this ApoE antibody.
Purity Antigen affinity
Storage Aliquot the ApoE antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
Limitation This ApoE antibody is available for research use only.
Uniprot # P02649
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/apoe-antibody-apolipoprotein-e-f50536
Title ApoE Antibody (Apolipoprotein E)
Description 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.
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