Natural兔Actin protein (ab73630)

概述

  • 产品名称Natural兔Actin protein
  • 蛋白长度Full length protein

描述

  • 性质Natural
  • 来源Native
  • 氨基酸序列
    • 种属Rabbit
    • 额外的序列信息Purified from rabbit striated muscle

技术指标

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.

  • 应用

    Western blot

    SDS-PAGE

  • 纯度> 98 % SDS-PAGE.
    Purity:Greater than 98.0% as determined by: (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE.
  • 形式Lyophilised
  • 补充说明

    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...

制备和贮存

  • 稳定性和存储

    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

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

常规信息

  • 别名
    • 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
    • ACTS_HUMAN
    • 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
  • 功能Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
  • 疾病相关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.
  • 序列相似性Belongs to the actin family.
  • 细胞定位Cytoplasm > cytoskeleton.
  • Information by UniProt

Natural Rabbit Actin protein 图像

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

    Secondary
    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)参考文献

ab73630 has not yet been referenced specifically in any publications.

Product Wall

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