製品の概要

  • 製品名Anti-PRRT2 antibody
    PRRT2 一次抗体 製品一覧
  • 製品の詳細
    Mouse polyclonal to PRRT2
  • アプリケーション適用あり: WBmore details
  • 種交差性
    交差種: Human
  • 免疫原

    Full length human PRRT2 protein (AAH53594.1).

  • ポジティブ・コントロール
    • PRRT2 transfected 293T lysate.

製品の特性

  • 製品の状態Liquid
  • 保存方法Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
  • バッファーPreservative: None
    Constituents: 1X PBS, pH 7.2
  • Concentration information loading...
  • 精製度Protein G purified
  • ポリ/モノポリクローナル
  • アイソタイプIgG
  • 研究分野

アプリケーション

Our Abpromise guarantee covers the use of ab70420 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. Detects a band of approximately 30 kDa (predicted molecular weight: 35 kDa).

ターゲット情報

  • 関連疾患Episodic kinesigenic dyskinesia 1 (EKD1) [MIM:128200]: An autosomal dominant neurologic condition characterized by recurrent and brief attacks of abnormal involuntary movements, triggered by sudden voluntary movement. These attacks usually have onset during childhood or early adulthood and can involve dystonic postures, chorea, or athetosis. Note=The disease is caused by mutations affecting the gene represented in this entry. Disease-causing mutations that produce truncation of the C-terminus of the protein alter subcellular location, from plasma membrane to cytosplasm (PubMed:22101681).
    Convulsions, familial infantile, with paroxysmal choreoathetosis (ICCA) [MIM:602066]: A syndrome characterized by clinical features of benign familial infantile seizures and episodic kinesigenic dyskinesia. Benign familial infantile seizures is a disorder characterized by afebrile seizures occurring during the first year of life, without neurologic sequelae. Paroxysmal choreoathetosis is a disorder of involuntary movements characterized by attacks that occur spontaneously or are induced by a variety of stimuli. Note=The disease is caused by mutations affecting the gene represented in this entry.
    Seizures, benign familial infantile 2 (BFIS2) [MIM:605751]: An autosomal dominant disorder in which afebrile seizures occur in clusters during the first year of life, without neurologic sequelae. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • 配列類似性Belongs to the CD225/Dispanin family.
  • 細胞内局在Cell membrane. Cell junction > synapse.
  • Information by UniProt
  • 参照データベース
  • 別名
    • interferon induced transmembrane protein domain containing 1 antibody
    • BFIC2 antibody
    • BFIS2 antibody
    • Dispanin subfamily B member 3 antibody
    • DSPB3 antibody
    • DYT10 antibody
    • EKD1 antibody
    • FLJ25513 antibody
    • ICCA antibody
    • IFITMD1 antibody
    • PKC antibody
    • Proline rich transmembrane protein 2 antibody
    • Proline-rich transmembrane protein 2 antibody
    • PRRT2 antibody
    • PRRT2_HUMAN antibody
    see all

Anti-PRRT2 antibody 画像

  • All lanes : Anti-PRRT2 antibody (ab70420) at 1/500 dilution

    Lane 1 : PRRT2 transfected 293T lysate
    Lane 2 : Non-transfected 293T lysate

    Lysates/proteins at 25 µg per lane.

    Secondary
    Goat Anti-Mouse IgG (H&L)-HRP at 1/2500 dilution

    Predicted band size : 35 kDa
    Observed band size : 30 kDa (why is the actual band size different from the predicted?)

Anti-PRRT2 antibody (ab70420) 使用論文

ab70420 has not yet been referenced specifically in any publications.

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Da es sich bei diesem Antikörper um einen polyklonalen Antikörper handelt, der gegen gesamte Protein gerichtet ist, gibt es kein spezifisches Epitop: Dieser Antikörper ist ein Gemisch aus Antikör...

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