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PEX10 抗体

PEX10 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2458699
发货至: 中国
  • 抗原 See all PEX10 抗体
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    适用
    • 25
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    宿主
    • 38
    • 2
    克隆类型
    • 38
    • 2
    多克隆
    标记
    • 16
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    • 1
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    This PEX10 antibody is un-conjugated
    应用范围
    • 14
    • 13
    • 13
    • 13
    • 6
    • 5
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PEX10.
    Top Product
    Discover our top product PEX10 Primary Antibody
  • 应用备注
    PEX10 antibody can be used for detection of PEX10 by ELISA at 1:1562500. PEX10 antibody can be used for detection of PEX10 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store PEX10 antibody at -20 °C.
  • 抗原
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    别名
    PEX10 (PEX10 产品)
    别名
    ATPEX10 antibody, T9J22.2 antibody, peroxin 10 antibody, NALD antibody, PBD6A antibody, PBD6B antibody, RNF69 antibody, AV128229 antibody, Gm142 antibody, peroxin 10 antibody, peroxisomal biogenesis factor 10 antibody, PEX10 antibody, Pex10 antibody
    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.
    分子量
    37 kDa
    基因ID
    5192
    NCBI登录号
    NP_002608
    UniProt
    O60683
    途径
    Monocarboxylic Acid Catabolic Process
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