Cat: IPD-X29353

Recombinant Human MTFP1 Protein,GST

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Analytical Data

  • Gene name

    MTFP1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    Mitochondrial 18KDA protein

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- GST

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9UDX5

  • Expression Region

    1-166aa

  • Molecular Weight

    45 kDa

  • Endotoxin

    < 1.0 EU per μg protein as determined by the LAL method.

  • Form

    Freeze-dried powder

  • Buffer formulation

    PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.

  • Reconstitution

    Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.

  • Customization

    Site-directed mutagenesis Custom tag design Custom buffer formulation Custom full-length protein production

  • Stability Test

    The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.

  • Storage & Shelf Life

    Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.

  • Shipping

    In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.

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Protein Description

The MTFP1 (mitochondrial fission process 1) recombinant protein has garnered attention in the field of cellular and molecular biology due to its pivotal role in regulating mitochondrial dynamics, particularly in the process of mitochondrial fission. Mitochondria are essential organelles involved in energy production, metabolism, and apoptosis, and their dysfunction is linked to various diseases, including neurodegenerative disorders and metabolic syndrome. Understanding the mechanisms underlying mitochondrial dynamics is crucial for developing therapeutic strategies. Research indicates that MTFP1 is a key player in facilitating the fission process, as it aids in the recruitment of essential dynamin-related proteins that contribute to the division of mitochondria. Investigations into the protein's structure and function can reveal insights into how alterations in MTFP1 expression and activity may lead to mitochondrial-related pathologies. Furthermore, recombinant technology allows for the production of MTFP1 in controlled laboratory settings, enabling detailed studies on its interactions, regulatory mechanisms, and potential as a biomarker for mitochondrial dysfunction. The exploration of MTFP1's role in cellular processes not only enhances our understanding of mitochondrial biology but also opens avenues for innovative approaches in treating mitochondrial disorders by potentially targeting this protein to restore normal mitochondrial function.

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