Desmin Rabbit pAb, Cy5 conjugated(bs-1026R-Cy5)-100ul

Desmin Rabbit pAb, Cy5 conjuga

ted(bs-1026R-Cy5)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-1026R-Cy5
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-1026R-Cy5
    英文名称Desmin Rabbit pAb, Cy5 conjugated
    中文名称Cy5标记的结蛋白抗体
    英文别名DESM_HUMAN; DES;
    产品应用ICC/IF=1:50-200, IF=1:100-500

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human Desmin
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Cancer > Invasion/microenvironment > ECM > Extracellular matrix

    Cardiovascular > Heart > Cardiac arrhythmias

    Signal Transduction > Cytoskeleton / ECM > Cytoskeleton > Intermediate Filaments > Class III > Desmin

    Stem Cells > Mesenchymal Stem Cells > Myogenesis

    亚基Homopolymer. Interacts with DST. Interacts with MTM1.
    亚细胞定位Cytoplasm.
    翻译后修饰ADP-ribosylation prevents ability to form intermediate filaments.
    相似性Belongs to the intermediate filament family.
    功能Desmin are class-III intermediate filaments found in muscle cells. In adult striated muscle they form a fibrous network connecting myofibrils to each other and to the plasma membrane from the periphery of the Z-line structures.
    保存条件Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料Desmin is a muscle-specific, type III intermediate filament that integrates the sarcolemma, Z disk, and nuclear membrane in sarcomeres and regulates sarcomere architecture. In adult striated muscle they form a fibrous network connecting myofibrils to each other and to the plasma membrane from the periphery of the Z line structures. Defects in Desmin are the cause of desmin related cardio skeletal myopathy (CSM) also known as desmin related myopathy (DRM). CSM is characterized by skeletal muscle weakness associated with cardiac conduction blocks, arrhythmias, restrictive heart failure, and by intracytoplasmic accumulation of desmin reactive deposits in cardiac and skeletal muscle cells. A desmin related myopathy can have a distal onset, it is then known as hereditary distal myopathy (HDM). Defects in Desmin are also the cause of dilated cardiomyopathy type 1I (CMD1I). CMD1I is an autosomal form of dilated cardiomyopathy characterized by ventricular dilatation and impaired systolic function. Antidesmin antibodies are useful in identification of tumours of myogenic origin

     

    应用推荐稀释比例
    {ICC/IF}{1:50-200}
    {IF}{1:100-500}

     

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