Cat: PA1000-187DB

Recombinant Human AP1S2 Protein,His

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Analytical Data

  • Gene name

    AP1S2

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    AP1S2;AP-1 complex subunit sigma-2

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P56377

  • Expression Region

    1-157aa

  • AA Sequence

    MGSSHHHHHHSSGLVPRGSHMQFMLLFSRQGKLRLQKWYVPLSDKEKKKI TRELVQTVLARKPKMCSFLEWRDLKIVYKRYASLYFCCAIEDQDNELITL EIIHRYVELLDKYFGSVCELDIIFNFEKAYFILDEFLLGGEVQETSKKNV LKAIEQADLLQEEAETPRSVLEEIGLT

  • Molecular Weight

    21 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

AP1S2, also known as AP-1 complex subunit sigma-2, is a crucial component of the adaptor protein complex AP-1, which plays a significant role in intracellular trafficking and membrane biogenesis. Research into AP1S2 has gained prominence due to its involvement in various cellular processes, including endocytosis, exocytosis, and signaling pathways. Mutations and dysregulation of AP1S2 are linked to several diseases, including intellectual disabilities and other neurodevelopmental disorders. The importance of understanding AP1S2 is underscored by its potential as a therapeutic target and its role in cellular homeostasis. Studies have employed various techniques, including recombinant DNA technology, to produce and analyze AP1S2 protein, allowing researchers to explore its structure and function. The generation of recombinant AP1S2 has enabled detailed investigations into its interactions with other proteins and its role in the assembly and function of the AP-1 complex. As the field progresses, insights gained from AP1S2 research could contribute to the development of novel strategies for diagnosing and treating diseases linked to its dysfunction. Understanding the molecular mechanisms of AP1S2 will provide valuable knowledge regarding intracellular trafficking pathways, which are vital for maintaining cellular health and function.

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