APOE polyclonal, anti-human
€426.00
In stock
SKU
AC-AF1082a
Catalog Number: AC-AF1082a
Size: 100 µg
Isotype: Goat
Applications: WB, IHC, E
Datasheet
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Size: 100 µg
Isotype: Goat
Applications: WB, IHC, E
Datasheet
Request Information
Background:
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.
Other Names:
Apolipoprotein E, Apo-E, APOE
Antigen Types:
Synthetic Peptide
Gene Name:
APOE (HGNC:613)
Gene ID:
348
Primary Accession: P02649
Other Accession: NP_000032;348;
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.
Other Names:
Apolipoprotein E, Apo-E, APOE
Antigen Types:
Synthetic Peptide
Gene Name:
APOE (HGNC:613)
Gene ID:
348
Primary Accession: P02649
Other Accession: NP_000032;348;
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