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PEX14 抗体 (AA 151-250) (FITC)

This anti-PEX14 antibody is a 兔 多克隆 antibody detecting PEX14 in IF (cc) 和 IF (p). Suitable for 大鼠.
产品编号 ABIN6944502
发货至: 中国
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Quick Overview for PEX14 抗体 (AA 151-250) (FITC) (ABIN6944502)

抗原

See all PEX14 抗体
PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))

适用

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大鼠

宿主

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克隆类型

  • 64
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多克隆

标记

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This PEX14 antibody is conjugated to FITC

应用范围

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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

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    AA 151-250

    交叉反应

    大鼠

    预测反应

    Human,Mouse,Dog,Cow,Sheep,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human PEX14

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))

    别名

    PEX14

    背景

    Synonyms: dJ734G22.2, NAPP2, NF E2 associated polypeptide 2, Peroxin 14, Peroxin-14, Peroxisomal biogenesis factor 14, Peroxisomal membrane anchor protein PEX14, Peroxisomal membrane anchor protein Pex14p, Peroxisomal membrane protein PEX14, pex14, PEX14_HUMAN, Pex14p, PTS1 receptor docking protein, PTS1 receptor-docking protein.

    Background: This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome. [provided by RefSeq, Jul 2008]

    基因ID

    5195

    UniProt

    O75381

    途径

    Maintenance of Protein Location
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