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ABCG5 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN0482
产品名称
ABCG5 Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
ABCG5
蛋白名称
ATP-binding cassette sub-family G member 5 (Sterolin-1)
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Human Gene ID
64240
Human Swissprot No.
Q9H222
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q9H222/entry
Mouse Swissprot No.
Q99PE8
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q99PE8
Rat Swissprot No.
Q99PE7
Rat Swissprot Link
http://www.uniprot.org/uniprot/O54941Q99PE7
免疫原
Synthesized peptide derived from human protein . at AA range: 250-330
特异性
ABCG5 Polyclonal Antibody detects endogenous levels of protein.
稀释度
WB 1:500 - 1:2000. ELISA: 1:5000. IF 1:100-300 Not yet tested in other applications.
预测分子量
71kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
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],
组织表达
Strongly expressed in the liver, lower levels in the small intestine and colon.
细胞定位
Cell membrane ; Multi-pass membrane protein . Apical cell membrane ; Multi-pass membrane protein .
信号通路
ABC transporters;
功能
disease: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.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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