Product datasheet
Human ABCG5 peptide ab87830
Overview
Product name
Human ABCG5 peptide
Description
Nature
Synthetic
Specifications
Our Abpromise guarantee covers the use of ab87830 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Purity
70 - 90% by HPLC.
Form
Liquid
Preparation and Storage
Stability and Storage
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw
cycles.
Information available upon request.
General Info
Function
Transporter that appears to play an indispensable role in the selective transport of the dietary
cholesterol in and out of the enterocytes and in the selective sterol excretion by the liver into bile.
Tissue specificity
Strongly expressed in the liver, lower levels in the small intestine and colon.
Involvement in disease
Defects in ABCG5 are a cause of sitosterolemia (STSL) [MIM:210250]; also known as
phytosterolemia or shellfish sterolemia. It is a rare autosomal recessive disorder characterized
by increased intestinal absorption of all sterols including cholesterol, plant and shellfish sterols,
and decreased biliary excretion of dietary sterols into bile. Sitosterolemia patients have
hypercholesterolemia, very high levels of plant sterols in the plasma, and frequently develop
tendon and tuberous xanthomas, accelerated atherosclerosis and premature coronary artery
disease.
Sequence similarities
Belongs to the ABC transporter superfamily. ABCG family. Eye pigment precursor importer (TC
3.A.1.204) subfamily.
Contains 1 ABC transmembrane type-2 domain.
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Contains 1 ABC transporter domain.
Cellular localization
Membrane.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
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Terms and conditions
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