APOB Break Apart FISH Probe

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. [provided by RefSeq, Jul 2008]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
APOBBA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
APOBBA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
APOBBA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
APOBBA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
APOBBA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
APOBBA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
APOBBA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
APOBBA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

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. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol : APOB

Gene Name : Apolipoprotein B

Chromosome : CHR 2: 210,440,72-210,014,28

Locus : 2p24.1

Alt. Genes : AKAP9

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