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Recombinant Human ApoB protein

Cat NoADMD-029
Conjugate
Type重组蛋白
SourceE.Coli
TagN/A
Size1mg
ApplicationImmunology
FormatLiquid
ConcentrationPlease refer to the vial lable for the specific concentration.
BufferSupplied in PBS
SpeciesHuman
StorageStore at -20 degree. Avoid repeated freeze/thaw cycles.
SynonymsApo B 100;Apo B;Apo B-100;Apo B-48;ApoB 100;ApoB 48;ApoB;APOB protein;APOB_HUMAN;Apolipoprotein B 100;Apolipoprotein B 48;Apolipoprotein B;Apolipoprotein B-48;FLDB.
PurificationProtein A/G
MolecularWeight
Description
BackgroundInvolvement in disease: Defects in APOB are a cause of hypobetalipoproteinemia familial type 1 (FHBL1) . A disorder characterized by highly reduced plasma concentrations of low density lipoproteins, and dietary fat malabsorption. Clinical presentation may vary from no symptoms to severe gastrointestinal and neurological dysfunction similar to abetalipoproteinemia. Defects in APOB are a cause of familial ligand-defective apolipoprotein B-100 (FDB). FDB is a 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.
We can offer labeled proteins/antibodies using a broad range of intensely fluorescent dyes and labels including FITC, Biotin, Alexa Fluor, Rhodamine B, Cy, Co-Au.
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