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Last updated: 2016/10/16
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TNNT1 purified MaxPab mouse polyclonal antibody (B01P)MaxPab

  • Catalog # : H00007138-B01P
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length human TNNT1 protein.
  • Immunogen:
  • TNNT1 (NP_003274, 1 a.a. ~ 251 a.a) full-length human protein.
  • Sequence:
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Publication Reference
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • TNNT1 MaxPab polyclonal antibody. Western Blot analysis of TNNT1 expression in SJCRH30.
  • PDF DownloadProtocol Download
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of TNNT1 expression in transfected 293T cell line (H00007138-T01) by TNNT1 MaxPab polyclonal antibody.

    Lane 1: TNNT1 transfected lysate(27.61 KDa).
    Lane 2: Non-transfected lysate.
  • PDF DownloadProtocol Download
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 7138
  • Gene Name:
  • TNNT1
  • Gene Alias:
  • ANM,FLJ98147,MGC104241,STNT,TNT,TNTS
  • Gene Description:
  • troponin T type 1 (skeletal, slow)
  • Gene Summary:
  • This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • slow skeletal muscle troponin T,troponin T1, skeletal, slow,troponin-T1, skeletal, slow
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