Cat: PA1000-9784

Recombinant Human MYO7B Protein,His

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Analytical Data

  • Gene name

    MYO7B

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    MYO7B;Unconventional myosin-VIIb

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q6PIF6

  • Expression Region

    全长

  • AA Sequence

    full

  • 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

MYO7B (Myosin VIIB) is a member of the myosin superfamily of motor proteins, playing a crucial role in cellular processes, particularly in the transport and organization of cellular components. It is predominantly expressed in the inner ear and the retina, where it is essential for hair cell function and photoreceptor integrity. Mutations in the MYO7B gene have been linked to various auditory and visual disorders, including non-syndromic hearing loss and inherited retinal diseases. The study of MYO7B recombinant protein is vital for understanding its structure-function relationship, as well as its mechanisms of action. Investigating the protein’s interactions and pathways could reveal insights into the molecular underpinnings of associated diseases. Furthermore, MYO7B's potential as a therapeutic target or biomarker emphasizes the importance of recombinant protein research, facilitating the development of gene therapies or interventions aimed at correcting the functional deficits caused by MYO7B mutations. By producing and characterizing MYO7B recombinant protein, researchers can elucidate the protein's role in cellular dynamics, paving the way for novel strategies in treating related auditory and visual impairments.

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