| Product Name | APOB Antibody |
|---|---|
| Description | Rabbit polyclonal antibody to APOB |
| Synonyms | Apo B 100 antibody; Apo B antibody; Apo B-100 antibody; Apo B-48 antibody; Apo B100 antibody; Apo B48 antibody; ApoB 100 antibody; ApoB 48 antibody; APOB antibody; APOB_HUMAN antibody; Apolipoprotein B (including Ag(x) antigen) antibody; Apolipoprotein B 100 antibody; Apolipoprotein B 48 antibody; Apolipoprotein B antibody; Apolipoprotein B-48 antibody; Apolipoprotein B100 antibody; Apolipoprotein B48 antibody; FLDB antibody; LDLCQ4 antibody |
| Host | Rabbit |
| Clonality | Polyclonal |
| Conjugate | Unconjugated |
| Immunogen | Synthetic peptide of human APOB |
| Isotype | IgG |
| Target | APOB |
| Reactivity | Human, Mouse, Rat |
| Applications | ELISA, IHC |
| Form | Liquid |
| Diluent Buffer | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Uniprot | P04114 |
| Storage | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. |
| Background | This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. It occurs in plasma as two main isoforms, apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2180 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. Mutations in this gene or its regulatory region cause hypobetalipoproteinemia, normotriglyceridemic hypobetalipoproteinemia, and hypercholesterolemia due to ligand-defective apoB, diseases affecting plasma cholesterol and apoB levels. |
| Supplier | Cusabio |
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