APOB, also named as Apo B-48 and Apo B-100, is a major protein constituent of chylomicrons (apo B-48), LDL (apo B-100) and VLDL (apo B-100). APOB functions as a recognition signal for the cellular binding and internalization of LDL particles by the apoB/E receptor. Defects in APOB are a cause of familial hypobetalipoproteinemia (FHBL). Defects in APOB are a cause of familial ligand-defective apolipoprotein B-100 (FDB). Defects in APOB associated with defects in other genes (polygenic) can contribute to hypocholesterolemia. The antibody is specific to APOB.
Western Blot: Mouse Liver Tissue, 1:200-1:2000; IHC: Human Liver Tissue, 1:20-1:200
Type: Primary
Antigen: APOB
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse