SCARB2 抗体
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- 抗原 See all SCARB2 抗体
- SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This SCARB2 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human SCARB2
- 亚型
- IgG
- Top Product
- Discover our top product SCARB2 Primary Antibody
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- 应用备注
- WB 1:1000 - 1:3000
- 限制
- 仅限研究用
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- 浓度
- 1 mg/mL
- 缓冲液
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))
- 别名
- SCARB2 (SCARB2 产品)
- 别名
- cd36l2 antibody, fi13c07 antibody, chunp6914 antibody, wu:fi13c07 antibody, SCARB2 antibody, scarb2 antibody, AMRF antibody, CD36L2 antibody, EPM4 antibody, HLGP85 antibody, LGP85 antibody, LIMP-2 antibody, LIMPII antibody, SR-BII antibody, 9330185J12Rik antibody, Cd36l2 antibody, MLGP85 antibody, LimpII antibody, scavenger receptor class B, member 2a antibody, scavenger receptor class B member 2 antibody, scavenger receptor class B, member 2 antibody, scarb2a antibody, SCARB2 antibody, scarb2 antibody, Scarb2 antibody
- 背景
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Synonyms: 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 (lysosomal integral membrane protein II),CD36 antigen,CD36 antigen-like 2,CD36L2,EPM4,HLGP85,LGP85,LIMP 2,LIMP II,LIMP2,LIMPII,Lysosomal integral membrane protein II,Lysosome membrane protein 2,Lysosome membrane protein II,OTTHUMP00000160590,OTTHUMP00000219176,Scarb2,Scavenger receptor class B member 2,Scavenger receptor class B, member 2,SCRB2,SR BII,SRBII
Background: The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
- 分子量
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Observed_MW: 80kDa
Calculated_MW: 37kDa/54kDa
- 基因ID
- 950
- UniProt
- Q14108
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