製品の概要

  • 製品名Anti-Actin antibody
    Actin 一次抗体 製品一覧
  • 製品の詳細
    Rabbit polyclonal to Actin
  • アプリケーション適用あり: WB, IHC-Pmore details
  • 種交差性
    交差種: Rat, Human
    交差が予測される動物種: Mouse, a wide range of other species
  • 免疫原

    Synthetic peptide corresponding to Human Actin aa 365-375 (C terminal).
    Sequence:

    SGPSIVHRKCF

  • ポジティブ・コントロール
    • Rat cardiac muscle tissue. Lysate from rat cardiac muscle tissue, rat brain tissue, rat testis tissue, rat skeletal muscle tissue. Whole cell lysate prepared from MM231 cells, HeLa cells, SMMC cells, HT1080 cells, SW620 cells.

アプリケーション

Our Abpromise guarantee covers the use of ab95437 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 Use a concentration of 0.1 - 0.5 µg/ml. Predicted molecular weight: 42 kDa.
IHC-P Use a concentration of 0.5 - 1 µg/ml. 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Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
  • 関連疾患Defects in ACTA1 are the cause of nemaline myopathy type 3 (NEM3) [MIM:161800]. A form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-or rod-like structures in muscle fibers on histologic examination. The phenotype at histological level is variable. Some patients present areas devoid of oxidative activity containg (cores) within myofibers. Core lesions are unstructured and poorly circumscribed.
    Defects in ACTA1 are a cause of myopathy congenital with excess of thin myofilaments (MPCETM) [MIM:161800]. A congenital muscular disorder characterized at histological level by areas of sarcoplasm devoid of normal myofibrils and mitochondria, and replaced with dense masses of thin filaments. Central cores, rods, ragged red fibers, and necrosis are absent.
    Defects in ACTA1 are a cause of congenital myopathy with fiber-type disproportion (CFTD) [MIM:255310]; also known as congenital fiber-type disproportion myopathy (CFTDM). CFTD is a genetically heterogeneous disorder in which there is relative hypotrophy of type 1 muscle fibers compared to type 2 fibers on skeletal muscle biopsy. However, these findings are not specific and can be found in many different myopathic and neuropathic conditions.
  • 配列類似性Belongs to the actin family.
  • 細胞内局在Cytoplasm > cytoskeleton.
  • Information by UniProt
  • 参照データベース
  • 別名
    • a actin antibody
    • ACTA antibody
    • ACTA1 antibody
    • Actin alpha skeletal muscle antibody
    • Actin antibody
    • actin, alpha 1, skeletal muscle 1 antibody
    • actin, alpha 1, skeletal muscle antibody
    • Actin, alpha skeletal muscle antibody
    • actina antibody
    • actine antibody
    • ACTS_HUMAN antibody
    • aktin antibody
    • Alpha Actin 1 antibody
    • Alpha skeletal muscle Actin antibody
    • alpha skeletal muscle antibody
    • alpha-actin antibody
    • Alpha-actin-1 antibody
    • ASMA antibody
    • CFTD antibody
    • CFTD1 antibody
    • CFTDM antibody
    • MPFD antibody
    • NEM1 antibody
    • NEM2 antibody
    • NEM3 antibody
    • nemaline myopathy type 3 antibody
    see all

Anti-Actin antibody 画像

  • All lanes : Anti-Actin antibody (ab95437) at 0.5 µg/ml

    Lane 1 : Rat cardiac muscle missue lysate
    Lane 2 : Rat brain tissue lysate
    Lane 3 : Rat testis tissue lysate
    Lane 4 : Rat skeletal muscle tissue lysate
    Lane 5 : MM231 cell lysate
    Lane 6 : HeLa cell lysate
    Lane 7 : SMMC cell lysate
    Lane 8 : HT1080 cell lysate
    Lane 9 : SW620 cell lysate

    Developed using the ECL technique

    Predicted band size : 42 kDa
  • ab95437 at 2µg/ml staining Actin in rat cardiac muscle tissue by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). A heat mediated antigen retrieval step was performed.

Anti-Actin antibody (ab95437) 使用論文

This product has been referenced in:
  • Carpinelli MR  et al. A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination. Dis Model Mech 7:649-57 (2014). WB ; Mouse . Read more (PubMed: 24682784) »

See 1 Publication for this product

Product Wall

Abcam has not validated the combination of species/application used in this Abreview.
Application Western blot
Sample Mouse Tissue lysate - whole (bones, skin, lung)
Gel Running Conditions Reduced Denaturing (4-12% Bis Tris)
Loading amount 50 µg
Specification bones, skin, lung
Blocking step BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 20°C
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投稿 Mar 08 2016

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