Cat: IPD-X26635

Recombinant Human Draxin Protein,His & SUMO

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Analytical Data

  • Gene name

    Draxin

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    Dorsal inhibitory axon guidance protein Dorsal repulsive axon guidance protein Neucrin

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His-SUMO

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q8NBI3

  • Expression Region

    26-349aa

  • Molecular Weight

    52 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

Draxin is a recently identified protein that plays a critical role in neuronal development and regeneration. Initially discovered during studies focused on understanding the molecular mechanisms underlying spinal cord repair, Draxin has emerged as a significant player in the guidance of neural progenitor cells and axonal growth. Its expression is notably high in the developing nervous system, indicating its involvement in key processes such as cell migration and differentiation. Researchers have also noted its potential interaction with various signaling pathways, which may provide insights into its function in neural regeneration. The exploration of Draxin as a recombinant protein has garnered attention for its therapeutic implications, particularly in treating neurodegenerative diseases and spinal cord injuries. As scientists delve deeper into its structure and interactions, the potential to leverage Draxin's properties to enhance neuronal survival and promote functional recovery becomes increasingly promising. Understanding the precise mechanisms through which Draxin operates will not only illuminate fundamental aspects of neurobiology but also pave the way for novel strategies in regenerative medicine. This research is paramount as the increasing prevalence of neurological disorders calls for innovative solutions to restore lost functions and improve patient outcomes.

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