清道夫受体B2抗体
规格：1mg/1ml
英文名： Scavenger Receptor BII
别名： 85 kDa lysosomal membrane sialoglycoprotein; 85 kDa lysosomal sialoglycoprotein scavenger receptor class B member 2; AMRF; CD36; CD36 antigen (collagen type I receptor, thrombospondin receptor)-like 2
分子量： 52kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：Polyclonal
亚型：IgG
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthetic peptide derived from human Scavenge
交叉反应：Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,
细胞定位：细胞浆 细胞膜
清道夫受体B2抗体产品介绍：background: High density lipoproteins (HDLs) play a critical role in cholesterol metabolism and their plasma concentrations are inversely correlated with risk for atherosclerosis. SR-BI and SR-BII (previously known as SR-BI.2) are the alternatively spliced products of a single gene. SR-BII and SR-BI are identical except for the encoded c-terminal cytoplasmic domain. Both SR-BI and SR-BII bind HDL and mediates selective uptake of HDL cholesteryl ester, but with SR-BII having an approximately 4-fold lower efficiency than SR-BI. SR-BI and SR-BII are expressed primarily in liver and non-placental steroidgenic tissues. Although the role of these scavenger receptors is not completely clear, SR-BII mRNA results from the alternative splicing of SR-BI precursor transcripts with both isoforms mediating selective transfer of lipid between HDL and cells. Therefore, the relative expression and functional activities of these two isoforms create a potential means of regulating selective lipid transfer between HDL and cells. Function: Acts as a lysosomal receptor for glucosylceramidase (GBA) targeting. Subunit: Interacts with GBA (via the coiled-coil domain). Subcellular Location: Lysosome membrane; Multi-pass membrane protein. DISEASE: Defects in SCARB2 are the清道夫受体B2抗体 cause of progressive myoclonic epilepsy type 4 with or without renal failure (EPM4) [MIM:254900]. An autosomal recessive progressive myoclonic epilepsy associated with renal failure in some cases. Cognitive function is preserved. Myoclonus is a brief, involuntary twitching of a muscle or a group of muscles. Cognitive function is preserved. Note=Genetic variants in SCARB2 can act as modifier of the phenotypic 清道夫受体B2抗体expression and severity of Gaucher disease. Similarity: Belongs to the CD36 family. Database links: Entrez Gene: 950 Human Entrez Gene: 12492 Mouse Entrez Gene: 117106 Rat Omim: 602257 Human SwissProt: Q14108 Human SwissProt: O35114 Mouse SwissProt: P27615 Rat Unigene: 349656 Human Unigene: 297964 Mouse Unigene: 3957 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
清道夫受体B2抗体产品应用：WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
研究领域：肿瘤 心血管 细胞生物 信号转导 转录调节因子 细胞膜受体
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid