Cat: IPD-X38995

Recombinant Human EPB42 Protein,His & GST

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Analytical Data

  • Gene name

    EPB42

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    PA; Erythrocyte Surface Protein Band 4.2

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His & GST

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P16452

  • Expression Region

    Leu475~Ala686

  • Molecular Weight

    54kDa

  • 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.

Quality inspection process

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Protein Description

EPB42, or erythrocyte membrane protein band 4.2, is a critical component of the erythrocyte cytoskeleton that plays a vital role in maintaining the structural integrity and stability of red blood cells. This protein is essential for the interaction between the cytoskeleton and the plasma membrane, contributing to the overall shape and flexibility of erythrocytes. Mutations or deficiencies in EPB42 have been implicated in various hematological disorders, including hereditary elliptocytosis and spheroidal disorders, which can lead to anemia and increased susceptibility to hemolysis. Research into EPB42 recombinants has gained traction in recent years, as scientists seek to elucidate its precise molecular mechanisms and interactions within the erythrocyte. Advances in recombinant DNA technology allow for the production of EPB42 in a laboratory setting, facilitating detailed studies of its structural and functional properties. Understanding EPB42’s role at the molecular level can potentially lead to the development of novel therapeutic approaches for related blood disorders. Moreover, studying EPB42 can provide insights into the broader mechanisms of membrane protein function and cytoskeletal dynamics, which are crucial for normal cellular physiology and can influence various pathophysiological conditions.

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