Overview

Description

  • NatureRecombinant
  • SourceEscherichia coli
  • Amino Acid Sequence
    • AccessionP19237
    • SpeciesHuman
    • Molecular weight24 kDa including tags
    • Amino acids1 to 187
    • TagsHis tag N-Terminus

Specifications

Our Abpromise guarantee covers the use of ab125609 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    Western blot

    SDS-PAGE

  • Purity> 75 % Densitometry.
    Purity determined to be >75% by densitometry.
  • FormLiquid
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 7.00
    Preservative: 1.02% Imidazole
    Constituents: 0.002% PMSF, 0.81% Sodium phosphate, 0.03% DTT, 25% Glycerol, 1.75% Sodium chloride

General Info

  • Alternative names
    • 2700018B22Rik
    • AI747285
    • DKFZp451O223
    • si:dz182n13.3
    • slow skeletal muscle
    • slow-twitch isoform
    • SSTNI
    • TNN1
    • Tnni1
    • TNNI1_HUMAN
    • Troponin I
    • Troponin I slow skeletal muscle
    • Troponin I slow twitch isoform
    • troponin I type 1 (skeletal, slow)
    • Troponin I, slow isoform
    see all
  • FunctionTroponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.
  • Tissue specificityHighest levels observed in human skeletal muscle (e.g. gastrocnemious muscle), differentiated cultures of primary human muscle cells and rhabdomyosarcoma cells cultured in low serum medium. Expressed in C2 muscle cell myoblasts and myotubes.
  • Sequence similaritiesBelongs to the troponin I family.
  • Information by UniProt

Recombinant Human TNNI1 protein images

  • SDS-PAGE analysis of ab125609.

References for Recombinant Human TNNI1 protein (ab125609)

ab125609 has not yet been referenced specifically in any publications.

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