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PEX10 抗体 (Middle Region)

This anti-PEX10 antibody is a 兔 多克隆 antibody detecting PEX10 in WB 和 IHC. Suitable for 人.
产品编号 ABIN310466
发货至: 中国

Quick Overview for PEX10 抗体 (Middle Region) (ABIN310466)

抗原

See all PEX10 抗体
PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

适用

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宿主

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克隆类型

  • 40
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多克隆

标记

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This PEX10 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

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    Middle Region

    序列

    QALRPDPLRV LMSVAPSALQ LRVRSLPGED LRARVSYRLL GVISLLHLVL

    预测反应

    Human: 100%

    产品特性

    This is a rabbit polyclonal antibody against PEX10. It was validated on Western Blot and immunohistochemistry.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human PEX10
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 346 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

    别名

    PEX10

    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: HNRNPD, PEX5, PEX14, LIG4, PCGF6, CGRRF1, MKRN3, PEX19, PEX12, PEX10, UBC, UBE2I, PEX2,
    Protein Size: 346

    分子量

    39 kDa

    基因ID

    5192

    NCBI登录号

    NM_153818, NP_722540

    途径

    Monocarboxylic Acid Catabolic Process
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