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PEX3 抗体 (AA 12-61)

The 兔 多克隆 anti-PEX3 antibody is suitable to detect PEX3 in samples from 人, 小鼠 和 大鼠. It has been validated for WB, IHC 和 ELISA.
产品编号 ABIN1535149
发货至: 中国
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Quick Overview for PEX3 抗体 (AA 12-61) (ABIN1535149)

抗原

See all PEX3 抗体
PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

适用

  • 19
  • 11
  • 10
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
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人, 小鼠, 大鼠

宿主

  • 15
  • 4
兔

克隆类型

  • 17
  • 2
多克隆

标记

  • 18
  • 1
This PEX3 antibody is un-conjugated

应用范围

  • 17
  • 11
  • 9
  • 1
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Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • 抗原表位

    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 12-61

    原理

    Peroxin 3 Antibody

    特异性

    Peroxin 3 Polyclonal Antibody detects endogenous levels of Peroxin 3 protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    纯度

    > 95 %

    免疫原

    The antiserum was produced against synthesized peptide derived from human PEX3. AA range:12-61

    亚型

    IgG
  • 应用备注

    WB 1:500-2000,IHC 1:50-300, ELISA 2000-20000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    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/1 year

    有效期

    12 months
  • 抗原

    PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

    别名

    PEX3

    背景

    Synonyms: PEX3, Peroxisomal biogenesis factor 3, Peroxin-3, Peroxisomal assembly protein PEX3

    Background: The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 20

    Gene Name: PEX3

    Protein Name: Peroxisomal biogenesis factor 3

    分子量

    42 kDa

    基因ID

    8504

    OMIM

    214100

    UniProt

    P56589
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