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SCARB2 抗体 (AA 200-380)

This anti-SCARB2 antibody is a 兔 多克隆 antibody detecting SCARB2 in WB. Suitable for 人.
产品编号 ABIN6147412
发货至: 中国

Quick Overview for SCARB2 抗体 (AA 200-380) (ABIN6147412)

抗原

See all SCARB2 抗体
SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))

适用

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宿主

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克隆类型

  • 45
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多克隆

标记

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This SCARB2 antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    AA 200-380

    序列

    GLFYEKNGTN DGDYVFLTGE DSYLNFTKIV EWNGKTSLDW WITDKCNMIN GTDGDSFHPL ITKDEVLYVF PSDFCRSVYI TFSDYESVQG LPAFRYKVPA EILANTSDNA GFCIPEGNCL GSGVLNVSIC KNGAPIIMSF PHFYQADERF VSAIEGMHPN QEDHETFVDI NPLTGIILKA A

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 200-380 of human SR-B2/LIMPII (NP_005497.1).

    亚型

    IgG
  • 应用备注

    WB,1:1000 - 1:3000

    说明

    HIGH QUALITY

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    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.
  • 抗原

    SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))

    别名

    SCARB2

    背景

    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.,SCARB2,AMRF,CD36L2,EPM4,HLGP85,LGP85,LIMP-2,LIMPII,SR-BII,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Cholesterol Metabolism,Cardiovascular,Lipids,SCARB2

    分子量

    37 kDa/54 kDa

    基因ID

    950

    UniProt

    Q14108
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