功能： disease:Defects in SCARB2 are the cause of action myoclonus-renal failure syndrome (AMRF) [MIM:254900]; also known as myoclonus-nephropathy syndrome. AMRF is an autosomal recessive progressive myoclonic epilepsy associated with renal failure. Myoclonus is a brief, involuntary twitching of a muscle or a group of muscles. Cognitive function is preserved.,function:May act as a lysosomal receptor.,mass spectrometry: PubMed:11840567,similarity:Belongs to the CD36 family.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Lysosome membrane ; Multi-pass membrane protein .
组织表达： Cerebellum,Eye,Liver,Mammary cancer,
科研货号： PLA007868
SCRB2 Polyclonal Antibody
Catalog NoPLA007868
Product information
基因名称： SCARB2 CD36L2 LIMPII
蛋白名称： Lysosome membrane protein 2 (85 kDa lysosomal membrane sialoglycoprotein) (LGP85) (CD36 antigen-like 2) (Lysosome membrane protein II) (LIMP II) (Scavenger receptor class B member 2) (CD antigen CD36)
功能： disease:Defects in SCARB2 are the cause of action myoclonus-renal failure syndrome (AMRF) [MIM:254900]; also known as myoclonus-nephropathy syndrome. AMRF is an autosomal recessive progressive myoclonic epilepsy associated with renal failure. Myoclonus is a brief, involuntary twitching of a muscle or a group of muscles. Cognitive function is preserved.,function:May act as a lysosomal receptor.,mass spectrometry: PubMed:11840567,similarity:Belongs to the CD36 family.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Lysosome membrane ; Multi-pass membrane protein .
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