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Last updated: 2017/1/22

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TCAP (Human) Recombinant Protein (P01)

  • Catalog # : H00008557-P01
  • Visit Frequency :
  • Countries :
  • Specification
  • Product Description:
  • Human TCAP full-length ORF ( AAH13330, 1 a.a. - 167 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • MATSELSCEVSEENCERREAFWAEWKDLTLSTRPEEGCSLHEEDTQRHETYHQQGQCQVLVQRSPWLMMRMGIHGRGLQEYQLPYQRVLPLPIFTPAKMGATKEEREDTPIQLQELLALETALGGQCVDRQEVAEITKQLPPVVPVSKPGALRRSLSRSMSQEAQRG
  • Host:
  • Wheat Germ (in vitro)
  • Theoretical MW (kDa):
  • 44.11
  • Purification:
  • Glutathione Sepharose 4 Fast Flow
  • Quality Control Testing:
  • 12.5% SDS-PAGE Stained with Coomassie Blue.

    QC Testing of H00008557-P01
  • Storage Buffer:
  • 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • Best use within three months from the date of receipt of this protein.
  • Applications
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Gene Information
  • Entrez GeneID:
  • 8557
  • Gene Name:
  • TCAP
  • Gene Alias:
  • CMD1N,LGMD2G,T-cap,TELE,telethonin
  • Gene Description:
  • titin-cap (telethonin)
  • Gene Summary:
  • Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. This gene encodes a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G. [provided by RefSeq
  • Other Designations:
  • 19 kDa sarcomeric protein,limb girdle muscular dystrophy 2G (autosomal recessive),telethonin
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