Cat: IPD-X27600

Recombinant Human TUBB4A Protein,His

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Analytical Data

  • Gene name

    TUBB4A

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    Tubulin 5 beta Tubulin beta-4 chain

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P04350

  • Expression Region

    1-444aa

  • Molecular Weight

    53.6 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

TUBB4A, a member of the beta-tubulin family, plays a crucial role in the formation and stability of microtubules, which are essential components of the cytoskeleton in eukaryotic cells. Mutations in the TUBB4A gene have been linked to various neurological disorders, including hypomyelinating leukodystrophy, which affects myelin sheath development in the central nervous system. Understanding TUBB4A’s structure and function has gained significant attention, as it can provide insights into the molecular mechanisms underlying these diseases. Researchers have focused on developing recombinant TUBB4A proteins to study their biochemical properties and interactions with other proteins. By producing TUBB4A in various expression systems, scientists aim to investigate how specific mutations alter its function, affecting microtubule dynamics and ultimately contributing to the pathophysiology of related disorders. This research not only enhances our understanding of TUBB4A itself but also contributes to the wider field of neurobiology and potential therapeutic avenues for diseases caused by cytoskeletal dysfunction.

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