Cat: IPD-X38550

Recombinant Human ABCA12 Protein,His

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Analytical Data

  • Gene name

    ABCA12

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    ABC-A12; LI2; ICR2B; Ichthyosis Congenita II,Lamellar Ichthyosis B; ATP-binding cassette sub-family A member 12

  • Species

    Human

  • Source

    E. coli

  • Tag

    N-His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q86UK0

  • Expression Region

    Val1346~Thr1577

  • Molecular Weight

    29kDa

  • 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

ABCA12 is a member of the ATP-binding cassette (ABC) transporter family, which plays a crucial role in lipid metabolism and cellular homeostasis. It is predominantly expressed in the epidermis and is essential for the formation of the skin barrier. Mutations in the ABCA12 gene are linked to a rare and severe skin disorder called harlequin ichthyosis, characterized by extreme skin dryness and scaling. Researchers have focused on the characterization of ABCA12 recombinant proteins to gain insights into its structure-function relationships and the molecular mechanisms underlying its role in keratinocyte lipid transport and epidermal differentiation. By utilizing various recombinant protein expression systems, scientists aim to produce functional ABCA12 proteins for biochemical and biophysical analysis, which may provide critical information about the domains responsible for substrate binding and transport. Understanding the dynamics of ABCA12 can pave the way for the development of therapeutic strategies for ichthyosis and related skin disorders, as well as advance the broader field of ABC transporter research, highlighting the importance of lipid transport in human health.

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