Cat: IPD-X28441

Recombinant Human KCNJ2 Protein (HEK293),His & Flag

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Analytical Data

  • Gene name

    KCNJ2

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    IRK1

  • Species

    Human

  • Source

    HEK293

  • Tag

    His;MBP;Flag

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P63252

  • Expression Region

    M1-I427

  • Protein Length

    Full Length

  • 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

KCNJ2, a member of the inward rectifier potassium channel family, plays a crucial role in maintaining cardiac and neuronal excitability by regulating potassium ion flow across cell membranes. Mutations in the KCNJ2 gene have been associated with various genetic disorders, most notably Andersen-Tawil syndrome, characterized by cardiac arrhythmias, periodic paralysis, and dysmorphic features. The study of KCNJ2 recombinant proteins has emerged as a vital avenue for understanding the structure-function relationships of this ion channel and for elucidating the pathophysiological mechanisms underlying KCNJ2-related diseases. By producing and characterizing recombinant KCNJ2 protein, researchers aim to investigate its biophysical properties, ion conductance, and the effects of specific mutations on its function. Such studies not only enhance our comprehension of KCNJ2's role in cellular physiology but also facilitate the development of targeted therapeutic strategies for conditions linked to KCNJ2 dysfunction. Advances in techniques such as X-ray crystallography and cryo-electron microscopy have further propelled this research area, providing insights into the ion channel's architecture and opening new avenues for drug discovery. Overall, the investigation of KCNJ2 recombinant proteins represents a critical intersection of molecular biology, genetics, and medicine, highlighting the importance of ion channels in health and disease.

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