cTnT/Troponin T Antibody Blocking Peptide(bs-2804P)-500ug

cTnT/Troponin T Antibody Block

ing Peptide(bs-2804P)-500ug
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  • ¥800
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  • bs-2804P
  • 2025年10月16日
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      500ug

    产品编号bs-2804P
    英文名称cTnT/Troponin T Antibody Blocking Peptide
    中文名称心肌特异性肌钙蛋白T封闭多肽
    英文别名Cardiac muscle troponin T; Cardiomyopathy dilated 1D (autosomal dominant); Cardiomyopathy hypertrophic 2; CMD1D; CMH2; CMPD2; cTnT; LVNC6; MGC3889; OTTHUMP00000033864; OTTHUMP00000033865; OTTHUMP00000033866; OTTHUMP00000033867; OTTHUMP00000033870; OTTHUMP00000218095; RCM3; TNNT 2; TNNT2; TNNT2_HUMAN; TnTC; Troponin T cardiac muscle; Troponin T type 2 (cardiac); Troponin T type 2 cardiac; Troponin T, cardiac muscle; Troponin T2; Troponin T2 cardiac.
    性状Lyophilized
    纯化方法HPLC
    研究领域

    Cardiovascular > Cardiovascular Markers > Cell Markers > Cardiomyocytes

    Cardiovascular > Heart > Contractility > Contractile Proteins > Troponin

    Signal Transduction > Cytoskeleton / ECM > Cytoskeleton > Microfilaments > Actin etc > Troponin

    Stem Cells > Mesenchymal Stem Cells > Myogenesis

    亚细胞定位Cytoplasm.
    组织特异性Heart. The fetal heart shows a greater expression in the atrium than in the ventricle, while the adult heart shows a greater expression in the ventricle than in the atrium. Isoform 6 predominates in normal adult heart. Isoforms 1, 7 and 8 are expressed in fetal heart. Isoform 7 is also expressed in failing adult heart.
    相似性Belongs to the troponin T family.
    功能Troponin T is the tropomyosin-binding subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.
    保存条件Shipped at 4℃. Stored at -20℃ 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The protein encoded by this gene is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy. Transcripts for this gene undergo alternative splicing that results in many tissue-specific isoforms, however, the full-length nature of some of these variants has not yet been determined. [provided by RefSeq].

     

     

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