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Peroxisomal Biogenesis Factor 10 (PEX10) Peptide

PEX10 适用: 人 宿主: 合成 BP, WB, IHC
产品编号 ABIN981595
发货至: 中国
  • 抗原 See all PEX10 products
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    宿主
    资源
    • 4
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-PEX10 antibody (Catalog #: ARP43442_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    别名
    ATPEX10 Peptide, T9J22.2 Peptide, peroxin 10 Peptide, NALD Peptide, PBD6A Peptide, PBD6B Peptide, RNF69 Peptide, AV128229 Peptide, Gm142 Peptide, peroxin 10 Peptide, peroxisomal biogenesis factor 10 Peptide, PEX10 Peptide, Pex10 Peptide
    背景
    PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.

    Alias Symbols: MGC1998, NALD, RNF69

    Protein Interaction Partner: PEX12,PEX19,PEX2,PEX5,PEX10,PEX12,PEX12,PEX19,PEX19,PEX2,PEX5

    Protein Size: 346
    分子量
    39 kDa
    基因ID
    5192
    NCBI登录号
    NM_153818, NP_722540
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