SKU: WP0907 Categories: ,

ABCG5 Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP0907-100
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Product details

Background:

The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. The protein encoded by this gene functions as a half-transporter to limit intestinal absorption and promote biliary excretion of sterols. It is expressed in a tissue-specific manner in the liver, colon, and intestine. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG8. Mutations in this gene may contribute to sterol accumulation and atheroschlerosis, and have been observed in patients with sitosterolemia. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetABCG5
ReactivityHuman, Mouse, Rat
ApplicationsWB, IF, ELISA
MW(Calculated)
MW(Observed)71kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; ELISA 1:5000; IF 1:100-300; Not yet tested in other applications.
FormulationLiquid in PBS containing 50% glycerol,0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human protein . at AA range: 250-330
SpecificityABCG5 Polyclonal Antibody detects endogenous levels of protein.
Gene NameABCG5
Protein NameATP-binding cassette sub-family G member 5 (Sterolin-1)
Other Name
SpeciesHuman
Gene ID64240
UniprotQ9H222,
Species.1Mouse
Gene ID.1
Uniprot.1Q99PE8,
Species.2Rat
Gene ID.2
Uniprot.2Q99PE7
Cellular LocalizationCell membrane; Multi-pass membrane protein . Apical cell membrane; Multi-pass membrane protein .
Tissue ExpressionStrongly expressed in the liver, lower levels in the small intestine and colon.
Signaling_pathway
Research Areas>>ABC transporters; / >>Fat digestion and absorption; / >>Bile secretion; / >>Cholesterol metabolism
FunctionDisease:Defects in ABCG5 are a cause of sitosterolemia [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.,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.,similarity:Belongs to the ABC transporter family. ABCG (White) subfamily.,similarity:Contains 1 ABC transmembrane type-2 domain.,similarity:Contains 1 ABC transporter domain.,subunit:May form heterodimers with ABCG8 or be tightly coupled to ABCG8 along a pathway regulating diatery-sterol absorption and excretion.,tissue specificity:Strongly expressed in the liver, lower levels in the small intestine and colon.,
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