Cat: IPD-X24845

Recombinant Human FIS1 Protein,His

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Analytical Data

  • Gene name

    FIS1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    CGI-135; TTC11; Tetratricopeptide Repeat Domain 11; Mitochondrial fission 1 protein

  • Species

    Human

  • Source

    E. coli

  • Tag

    N-His

  • Purity

    Greater than 95% as determined by SDS-PAGE.

  • Uniprot

    Q9Y3D6

  • Expression Region

    Met1~Ala117

  • Molecular Weight

    18kDa

  • 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

FIS1 ( mitochondrial fission 1) is a crucial protein involved in the regulation of mitochondrial dynamics, specifically in the process of mitochondrial fission, which is essential for maintaining cellular health and energy metabolism. Research into FIS1 has gained prominence due to its implications in various biological processes, including apoptosis, cellular proliferation, and inherited diseases. Understanding the mechanisms by which FIS1 interacts with other proteins and influences mitochondrial morphology is vital, as dysfunctional mitochondria have been linked to numerous pathologies, such as neurodegenerative disorders, metabolic syndromes, and cancer. Studies have shown that FIS1 plays a pivotal role in the recruitment of dynamin-related proteins, facilitating the division of mitochondria, and thereby enabling the distribution of mtDNA and organelles during cell division. Furthermore, alterations in FIS1 expression levels can lead to mitochondrial fragmentation, contributing to the onset of disease states. Consequently, researchers are focused on elucidating the regulatory pathways governing FIS1 function and exploring its potential as a therapeutic target. Insights gained from FIS1 research could lead to novel strategies for mitochondrial-related diseases, making it a significant focus in contemporary biomedical research.

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