製品の概要

  • 製品名Anti-PEX2 antibody
    PEX2 一次抗体 製品一覧
  • 製品の詳細
    Rabbit polyclonal to PEX2
  • アプリケーション適用あり: WB, IHC-Pmore details
  • 種交差性
    交差種: Human
  • 免疫原

    A synthesized peptide derived from N-terminal of Human PEX2

  • ポジティブ・コントロール
    • Human breast carcinoma tissue A549 cells

製品の特性

関連製品

アプリケーション

Our Abpromise guarantee covers the use of ab110004 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

アプリケーション Abreviews 特記事項
WB 1/500 - 1/1000. Predicted molecular weight: 35 kDa.
IHC-P 1/50 - 1/100. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.

ターゲット情報

  • 機能Somewhat implicated in the biogenesis of peroxisomes.
  • 関連疾患Defects in PEX2 are the cause of peroxisome biogenesis disorder complementation group 5 (PBD-CG5) [MIM:170993]; also known as PBD-CGF. PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). ZWS, NALD and IRD are distinct from RCDP and constitute a clinical continuum of overlapping phenotypes known as the Zellweger spectrum. The PBD group is genetically heterogeneous with at least 14 distinct genetic groups as concluded from complementation studies.
    Defects in PEX2 are a cause of Zellweger syndrome (ZWS) [MIM:214100]. ZWS is a fatal peroxisome biogenesis disorder characterized by dysmorphic facial features, hepatomegaly, ocular abnormalities, renal cysts, hearing impairment, profound psychomotor retardation, severe hypotonia and neonatal seizures. Death occurs within the first year of life.
    Defects in PEX2 are a cause of infantile Refsum disease (IRD) [MIM:266510]. IRD is a mild peroxisome biogenesis disorder (PBD). Clinical features include early onset, mental retardation, minor facial dysmorphism, retinopathy, sensorineural hearing deficit, hepatomegaly, osteoporosis, failure to thrive, and hypocholesterolemia. The biochemical abnormalities include accumulation of phytanic acid, very long chain fatty acids (VLCFA), di- and trihydroxycholestanoic acid and pipecolic acid.
  • 配列類似性Belongs to the pex2/pex10/pex12 family.
    Contains 1 RING-type zinc finger.
  • 細胞内局在Peroxisome membrane.
  • Information by UniProt
  • 参照データベース
  • 別名
    • 35 kDa peroxisomal membrane protein antibody
    • PAF-1 antibody
    • PAF1 antibody
    • Peroxin-2 antibody
    • peroxisomal biogenesis factor 2 antibody
    • Peroxisomal membrane protein 3 antibody
    • peroxisomal membrane protein 3, 35kDa antibody
    • Peroxisome assembly factor 1 antibody
    • Peroxisome biogenesis factor 2 antibody
    • PEX2 antibody
    • PEX2_HUMAN antibody
    • PMP3 antibody
    • PMP35 antibody
    • PXMP3 antibody
    • RING finger protein 72 antibody
    • RNF72 antibody
    • ZWS3 antibody
    see all

Anti-PEX2 antibody 画像

  • Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ab110004.
  • All lanes : Anti-PEX2 antibody (ab110004) at 1/500 dilution

    Lane 1 : A549 cells
    Lane 2 : A549 cells treated with the synthesized peptide

    Lysates/proteins at 5 µg per lane.


    Predicted band size : 35 kDa

Anti-PEX2 antibody (ab110004) 使用論文

ab110004 has not yet been referenced specifically in any publications.

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