Cat: IPD-X11578

Recombinant Human SMAD3 Protein(Baculovirus), N- His

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Analytical Data

  • Gene name

    SMAD3

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    JV15-2SMAD family member 3 ;SMAD 3 ;Smad3 ;hSMAD3

  • Species

    Human

  • Source

    Baculovirus

  • Tag

    N- His

  • Purity

    Greater than 85% as determined by SDS-PAGE.

  • Uniprot

    P84022

  • Expression Region

    1-425aa

  • Protein Length

    Partial

  • Molecular Weight

    50.6 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

SMAD3 is a critical intracellular signaling protein that plays a key role in the transformating growth factor-beta (TGF-β) signaling pathway, which is involved in various cellular processes including cell growth, differentiation, and apoptosis. Dysregulation of SMAD3 has been linked to a number of diseases, including fibrosis, cancer, and cardiovascular diseases. As a member of the SMAD family, SMAD3 transmits signals from TGF-β ligands to the nucleus, where it regulates gene expression by forming complexes with other transcription factors. The study of recombinant SMAD3 protein is essential for understanding its biochemical properties, interaction with other proteins, and its functional role in TGF-β signaling. Researchers often use recombinant SMAD3 to investigate its structure-function relationships and to screen for potential therapeutic targets, particularly in contexts where TGF-β signaling is aberrant. Furthermore, characterization of SMAD3 at the molecular level can provide insights into its mechanisms of action and offer potential avenues for therapeutic intervention in diseases linked to TGF-β signaling dysregulation. Overall, the exploration of SMAD3 as a recombinant protein not only enhances our understanding of its biological functions but also holds promise for developing novel strategies for treating TGF-β-related diseases.

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