Cat: IPD-X38698

Recombinant Human MYH16 Protein,His

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Analytical Data

  • Gene name

    MYH16

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Species

    Human

  • Source

    E. coli

  • Tag

    N-His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9H6N6

  • Expression Region

    Val209~Thr469

  • Molecular Weight

    32kDa

  • 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.

Quality inspection process

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Protein Description

MYH16 is a gene that encodes a myosin heavy chain protein, which plays a critical role in muscle contraction and is primarily expressed in skeletal muscle tissue. Research into MYH16 has gained attention due to its potential implications in various muscular and genetic disorders. Notably, mutations in the MYH16 gene have been associated with congenital myopathies, which can result in severe muscle weakness and developmental delays. The study of MYH16 recombinant proteins is particularly important for understanding the functional properties of the myosin heavy chain family and elucidating the molecular mechanisms underlying muscle contraction. Additionally, recombinant MYH16 proteins can serve as valuable tools for drug discovery, providing insights into therapeutic targets for muscle-related diseases. Recent advancements in genetic engineering techniques have facilitated the production of these recombinant proteins, allowing researchers to investigate their structural and functional characteristics in vitro. This research not only enhances our understanding of muscle physiology but also paves the way for potential clinical applications, including gene therapy and regenerative medicine. Overall, MYH16 represents a significant focus within muscle biology, highlighting its importance in both basic research and translational applications in the field of muscle pathologies.

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