本公司产品仅供体外研究使用,不用于临床诊断

ACTA1 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-14550

宿主: Rabbit

反应性: H,M,R

应用: WB,IHC

  • 详情
  • Overview

    Synonyms a actin,ACTA,ACTA1,Actin alpha skeletal muscle,Actin,actin,alpha 1,skeletal muscle 1,actin,alpha 1,skeletal muscle,Actin,alpha skeletal muscle,actina,actine,ACTS,aktin,Alpha Actin 1,Alpha skeletal muscle Actin,alpha skeletal muscle,alpha-actin,Alpha-actin-1,ASMA,CFTD,CFTD1,CFTDM,MPFD,NEM1,NEM2,NEM3,nemaline myopathy type 3,ACTA1抗体
    Swissprot P68133
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Recombinant protein of human ACTA1
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:50-1:200;
    Concentration 0.5 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cytoplasm
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
    Background The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.
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