Product Name
Apo B-100/48, Polyclonal Antibody
Full Product Name
Anti-Human Apo B-100/48 (Goat Polyclonal) Antibody
Product Synonym Names
Anti-Human Apo B-100/48 (Goat Polyclonal)
Product Gene Name
anti-Apo B-100/48 antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Chromosome Location
Chromosome: 2; NC_000002.11 (21224301..21266945, complement). Location: 2p24-p23
3D Structure
ModBase 3D Structure for P04114
Specificity
Specifically binds to human apo B-100/48.
Concentration
100ug/100ul (lot specific)
Immunogen
Apo B-100/48 recombinant protein.
Storage Buffer
PBS, pH 7.4 with 0.05% sodium azide.
Preparation and Storage
This product is stable for several weeks at 4 degree C as an undiluted liquid. Dilute only prior to immediate use. For extended storage, aliquot contents and freeze at -20 degree C or below. Avoid cycles of freezing and thawing. Expiration date is one (1) year from date of receipt.
Other Notes
Small volumes of anti-Apo B-100/48 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Product Categories/Family for anti-Apo B-100/48 antibody
Cholesterol Related Antibodies
Applications Tested/Suitable for anti-Apo B-100/48 antibody
ELISA (EIA)
Application Notes for anti-Apo B-100/48 antibody
Dilution for immunoblot and ELISA range: 1:500 to 1:1,000.
NCBI/Uniprot data below describe general gene information for Apo B-100/48. It may not necessarily be applicable to this product.
NCBI Accession #
NP_000375.2
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NCBI GenBank Nucleotide #
NM_000384.2
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UniProt Primary Accession #
P04114
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UniProt Secondary Accession #
O00502; P78479; P78480; P78481; Q13779; Q13785; Q13786; Q13787; Q13788; Q4ZG63; Q53QC8[Other Products]
UniProt Related Accession #
P04114[Other Products]
Molecular Weight
515,605 Da
NCBI Official Full Name
apolipoprotein B-100
NCBI Official Synonym Full Names
apolipoprotein B
NCBI Official Symbol
APOB??[Similar Products]
NCBI Official Synonym Symbols
FLDB; LDLCQ4
??[Similar Products]
NCBI Protein Information
apolipoprotein B-100; apoB-48; apoB-100; apo B-100; mutant Apo B 100; apolipoprotein B48; apolipoprotein B (including Ag(x) antigen)
UniProt Protein Name
Apolipoprotein B-100
UniProt Gene Name
APOB??[Similar Products]
UniProt Synonym Gene Names
Apo B-100; Apo B-48??[Similar Products]
UniProt Entry Name
APOB_HUMAN
NCBI Summary for Apo B-100/48
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]
UniProt Comments for Apo B-100/48
Function: Apolipoprotein B is a major protein constituent of chylomicrons (apo B-48), LDL (apo B-100) and VLDL (apo B-100). Apo B-100 functions as a recognition signal for the cellular binding and internalization of LDL particles by the apoB/E receptor.
Subunit structure: Interacts with PCSK9. Ref.38
Subcellular location: Cytoplasm. Secreted Ref.38.
Induction: Up-regulated in response to enterovirus 71 (EV71) infection (at protein level). Ref.34
Post-translational modification: Palmitoylated; structural requirement for proper assembly of the hydrophobic core of the lipoprotein particle. Ref.31
Involvement in disease: Familial hypobetalipoproteinemia 1 (FHBL1) [MIM:107730]: A disorder of lipid metabolism characterized by less than 5th percentile age- and sex-specific levels of low density lipoproteins, and dietary fat malabsorption. Clinical presentation may vary from no symptoms to severe gastrointestinal and neurological dysfunction similar to abetalipoproteinemia.Note: The disease is caused by mutations affecting the gene represented in this entry. Ref.46Familial ligand-defective apolipoprotein B-100 (FDB) [MIM:144010]: Dominantly inherited disorder of lipoprotein metabolism leading to hypercholesterolemia and increased proneness to coronary artery disease (CAD). The plasma cholesterol levels are dramatically elevated due to impaired clearance of LDL particles by defective APOB/E receptors.Note: The disease is caused by mutations affecting the gene represented in this entry. Ref.40 Ref.42 Ref.44 Ref.49Defects in APOB associated with defects in other genes (polygenic) can contribute to hypocholesterolemia.
Sequence similarities: Contains 1 vitellogenin domain.
RNA editing: Edited at position 2180.The stop codon (UAA) at position 2180 is created by RNA editing. Apo B-48, derived from the fully edited RNA, is produced only in the intestine and is found in chylomicrons. Apo B-48 is a shortened form of apo B-100 which lacks the LDL-receptor region. The unedited version (apo B-100) is produced by the liver and is found in the VLDL and LDL.
Sequence caution: The sequence AAA51752.1 differs from that shown. Reason: Frameshift at positions 942, 951, 1139, 1165, 1164, 1371 and 1385.
Research Articles on Apo B-100/48
1. There were significant associations between serum apoB, the apoB/apoA-I ratio and elevated CIMT. Serum apoB and the apoB/apoA-I ratio might be independent predictors of early atherosclerosis in NGT
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