製品の概要

  • 製品名Anti-USH2A antibody
    USH2A 一次抗体 製品一覧
  • 製品の詳細
    Rabbit polyclonal to USH2A
  • 特異性The antibody does not cross reacts with any other protein in RPE cells.
  • アプリケーション適用あり: WB, IPmore details
  • 種交差性
    交差種: Rat, Human
  • 免疫原

    Synthetic cyclic peptide:

    LTN REI LEV FSG DLL RLH AQS HC

    , corresponding to internal/mid region amino acids 280-302 of human USH2A.

  • ポジティブ・コントロール
    • This antibody strongly labels a 186 kDa protein in RPE (retinal pigment epithelium) cell extracts.

法規制情報

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. Avoid freeze / thaw cycles.
  • バッファーAntibody stabilization buffer, with preservatives, consisting of Hepes, NaCl, KCl, glycerol, BSA and chaotropic agents. Preservative: 0.01% Thimerosal (merthiolate)
  • Concentration information loading...
  • 精製度Immunogen affinity 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 ab42131 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. Detects a band of approximately 186 kDa.
IP 1/200.

ターゲット情報

  • 関連性The Usher 2A gene expresses an extra cellular matrix protein that resembles unconventional Myosin and do not appear to have any un-conventional functional correlations. It is expressed primarily in retina and cochlea and may be important in the development and homeostasis of the inner ear and retina. The human Usher Syndrome 2A (Ush2A) protein has several functional domains (Laminin type EGF like domain; Laminin-Type epidermal growth factor like domain and a fibronectin type 3 like domain). The protein has a single transmembrane domain that anchor the protein to the cell membrane, the rest of the protein stays outside the cell. Defects in the USH2A gene are the most common cause of deafness and blindness in adults and affect 3-6% children born with hearing impairments. The affected individuals have sensory-neural deficiencies at birth and subsequently develop progressive retinitis pigmentosa (RP). Three forms of Usher syndrome have been characterized, Usher Type 1, II and III which can be distinguish based on severity of hearing loss and vestibular involvement. Type I patents are profoundly deaf while type II (most common form of Usher syndrome) patients are mildly deaf but have normal in vestibular responses.
  • 細胞内局在Cell Membrane; single-pass type I membrane protein. Isoform 2 is secreted.
  • 参照データベース
  • 別名
    • dJ1111A8.1 antibody
    • US2 antibody
    • USH2A antibody
    • Usher syndrome type 2A protein antibody
    • Usher syndrome type IIa protein antibody
    • Usherin antibody
    see all

Anti-USH2A antibody (ab42131) 使用論文

ab42131 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"