Cat: PA2000-3525

Recombinant Human PAM16 Protein,His

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Analytical Data

  • Gene name

    PAM16

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    PAM16;MAGMAS;TIM16;TIMM16;Mitochondrial import inner membrane translocase subunit TIM16

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9Y3D7

  • Expression Region

    1-125aa

  • AA Sequence

    MAKYLAQIIVMGVQVVGRAFARALRQEFAASRAAADARGRAGHRSAAASNLSGLSLQEAQQILNVSKLSPEEVQKNYEHLFKVNDKSVGGSFYLQSKVVRAKERLDEELKIQAQEDREKGQMPHT

  • Molecular Weight

    40.8 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

PAM16, a mitochondrial protein, is part of the PAM complex involved in protein translocation across the inner mitochondrial membrane. Its role in facilitating the import of precursor proteins into the mitochondria is crucial for maintaining mitochondrial function and energy production. Dysfunction of PAM16 has been associated with various mitochondrial diseases, underscoring the importance of this protein in cellular metabolism and health. Recent studies have shown that PAM16 interacts with other components of the translocase of the inner mitochondrial membrane (TIM) complex, critical for understanding how proteins are folded and processed within mitochondria. Investigating PAM16 and its interactions may reveal insights into mitochondrial biogenesis, proper organelle functioning, and the molecular mechanisms underlying mitochondrial disorders. As research progresses, elucidating the precise mechanisms by which PAM16 operates could lead to potential therapeutic strategies aimed at treating diseases linked to mitochondrial dysfunction, thus emphasizing its significance in both basic research and clinical applications.

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