Natural Rabbit Actin protein (ab73630)


  • 製品名
    Natural Rabbit Actin protein
  • タンパク質長
    Full length protein


  • 由来
  • 由来
  • アミノ酸配列
    • 生物種
    • 配列の追加情報
      Purified from rabbit striated muscle


Our Abpromise guarantee covers the use of ab73630 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

    Western blot


  • 精製度
    > 98 % SDS-PAGE.
    Purity:Greater than 98.0% as determined by: (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE.
  • 製品の状態
  • 備考

    For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).

    ab73630 can be used in applications as a: Protein standard in 1D and 2D SDS gel electrophoresis Immunoassays Immunization

  • Concentration information loading...


  • 保存方法および安定性

    Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.00222% Calcium chloride, 0.5% SDS, 0.0154% DTT, 0.158% Tris HCl, 0.01014% ATP

  • 再構成
    Reconstitute in sterile 18MOhm/cm water to not less than 100µg/ml, which can then be further diluted to other aqueous solutions.


  • 別名
    • a actin
    • ACTA
    • ACTA1
    • Actin
    • Actin alpha skeletal muscle
    • actin, alpha 1, skeletal muscle
    • actin, alpha 1, skeletal muscle 1
    • Actin, alpha skeletal muscle
    • actina
    • actine
    • aktin
    • Alpha Actin 1
    • alpha skeletal muscle
    • Alpha skeletal muscle Actin
    • alpha-actin
    • Alpha-actin-1
    • ASMA
    • CFTD
    • CFTD1
    • CFTDM
    • MPFD
    • NEM1
    • NEM2
    • NEM3
    • nemaline myopathy type 3
    see all
  • 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

Natural Rabbit Actin protein 画像

  • Anti-Actin antibody - Loading Control (ab1801) at 1/1000 dilution + Natural Rabbit Actin protein (ab73630) at 0.1 µg

    Goat Anti-Rabbit IgG H&L (HRP) preadsorbed (ab97080) at 1/5000 dilution
    Developed using the ECL technique

    Performed under reducing conditions.

    Exposure time : 4 minutes

Natural Rabbit Actin protein (ab73630) 使用論文

ab73630 has not yet been referenced specifically in any publications.

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Thank you for your inquiry. This actin protein (ab73630) was purified from rabbit striated muscle and the purification method used results in a highly purified protein. Unfortunately, the protein of the muscle consists in the alpha-skeletal muscle ...

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