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Scavenger Receptor Class B, Member 2 (SCARB2) Peptide

SCARB2 适用: 哺乳动物 宿主: 合成 BP, WB, IHC
产品编号 ABIN936414
发货至: 中国
  • 抗原 See all SCARB2 products
    SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))
    蛋白类型
    Synthetic
    宿主
    哺乳动物
    资源
    • 5
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    序列
    VARVFQKAVD QSIEKKIVLR NGTEAFDSWE KPPLPVYTQF YFFNVTNPEE
    产品特性
    A synthetic peptide for use as a blocking control in assays to test for specificity of SCARB2 antibody,
    Alternative Names: SCARB2 control peptide, SCARB2 antibody Blocking Peptide, Anti-SCARB2 Blocking Peptide, scavenger receptor class B, member 2 Blocking Peptide, AMRF Blocking Peptide, CD36L2 Blocking Peptide, HLGP85 Blocking Peptide, LIMPII Blocking Peptide, SR-BII Blocking Peptide, SCARB2, SCARB-2, SCARB 2, SCARB-2 Blocking Peptide, SCARB 2 Blocking Peptide
  • 应用备注
    Optimal conditions should be determined by the investigator
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    缓冲液
    PBS
    注意事项
    Avoid repeated freeze/thaw cycles.
    储存条件
    -20 °C
    储存方法
    Store at -20 °C long term.
  • 抗原
    SCARB2 (Scavenger Receptor Class B, Member 2 (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).
    分子量
    53 kDa
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