Overview
- Product nameAnti-Apolipoprotein B antibody [7B8]See all Apolipoprotein B primary antibodies ...
- DescriptionMouse monoclonal [7B8] to Apolipoprotein B
- SpecificityAb39560 has specificity for Apolipoprotein B from serum/plasma. No crossreactivity is seen with Apolipoprotein A1.
- Tested applicationsELISA, WB more details
- Species reactivityReacts with: Human
- Immunogen
Human LDL.
Properties
- FormLiquid
- Storage instructionsStore at +4°C in the dark.
- Storage bufferPreservative: 15mM Sodium Azide
Constituents: 0.5M Sodium chloride, 0.01M PBS, pH 7.4 -
Concentration information loading... - PurityProtein A purified
- Clonality Monoclonal
- Clone number7B8
- Myelomax63-Ag8.653
- IsotypeIgG2b
- Light chain typekappa
- Research Areas
Applications
Our Abpromise guarantee covers the use of ab39560 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Notes |
|---|---|
| ELISA | ELISA: Use at an assay dependent dilution. Ab39560 reacts with Apolipoprotein B from human serum/plasma, when used in sandwich ELISA in combination with a polyclonal antibody against Apolipoprotein B, and also with isolated LDL directly coated onto the microtiter plate. |
| WB | WB: Use at an assay dependent dilution. Predicted molecular weight: 260 kDa. Ab39560 binds to Apolipoprotein B in reduced as well as in non-reduced forms, using isolated LDL as antigen. |
Target
- FunctionApolipoprotein 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.
- Involvement in diseaseFamilial 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.
Familial 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.
Note=Defects in APOB associated with defects in other genes (polygenic) can contribute to hypocholesterolemia. - Sequence similaritiesContains 1 vitellogenin domain.
- Post-translational
modificationsPalmitoylated; structural requirement for proper assembly of the hydrophobic core of the lipoprotein particle. - Cellular localizationCytoplasm. Secreted.
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Database links
- Entrez Gene: 338 Human
- Omim: 107730 Human
- SwissProt: P04114 Human
- Unigene: 120759 Human
Target information above from: UniProt accession
P04114
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010)
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Alternative names
- Apo B 100 antibodyApo B antibodyApo B-100 antibody
- Apo B-48 antibodyApoB 100 antibodyApoB 48 antibodyApoB antibodyAPOB protein antibodyAPOB_HUMAN antibodyApolipoprotein B 100 antibodyApolipoprotein B 48 antibodyApolipoprotein B antibodyApolipoprotein B-48 antibodyApolipoprotein B48 antibodyFLDB antibodyLDLCQ4 antibody
see all
References for Anti-Apolipoprotein B antibody [7B8] (ab39560)
ab39560 has not yet been referenced specifically in any publications.