Cat: IPD-X35164

Recombinant Human JAM-A/CD321 Protein (HEK293),His

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Analytical Data

  • Gene name

    JAM-A/CD321

  • 简介

    The JAM-A/CD321 protein is critical for the formation of epithelial tight junctions, is present in early junction development, and recruits PARD3. Binding of the PARD6-PARD3 complex may hinder PARD3-JAM1 interaction, thereby impeding tight junction assembly. JAM-A/CD321 Protein, Human (HEK293, His) is the recombinant human-derived JAM-A/CD321 protein, expressed by HEK293 , with C-6*His labeled tag.

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Biological Activity

    Immobilized Human JAM-A at 1 μg/mL (100 μL/well) can bind Anti-JAM-A antibody. The ED50 for this effect is 3.4 ng/mL. Immobilized Human JAM-A at 1 μg/mL (100 μL/well) can bind Anti-JAM-A antibody. The ED50 for this effect is 3.4 ng/mL.

  • Alternative Names

    Junctional Adhesion Molecule A; JAM-A; Junctional Adhesion Molecule 1; JAM-1; Platelet F11 Receptor; Platelet Adhesion Molecule 1; PAM-1; CD321; F11R; JAM1; JCAM

  • Species

    Human

  • Source

    HEK293

  • Tag

    C-6*His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9Y624-1

  • Expression Region

    S28-V238

  • AA Sequence

    SVTVHSSEPEVRIPENNPVKLSCAYSGFSSPRVEWKFDQGDTTRLVCYNNKITASYEDRVTFLPTGITFKSVTREDTGTYTCMVSEEGGNSYGEVKVKLIVLVPPSKPTVNIPSSATIGNRAVLTCSEQDGSPPSEYTWFKDGIVMPTNPKSTRAFSNSSYVLNPTTGELVFDPLSASDTGEYSCEARNGYGTPMTSNAVRMEAVERNVGV

  • Protein Length

    Extracellular Domain

  • Molecular Weight

    27-31kDa

  • 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

JAM-A (Junctional Adhesion Molecule A), also known as CD321, is a cell adhesion molecule predominantly expressed in endothelial cells and immune cells. It plays a crucial role in maintaining the integrity of tight junctions in epithelial and endothelial barriers, regulating leukocyte transmigration, and contributing to various physiological and pathological processes, including inflammation, tumor metastasis, and tissue regeneration. The research surrounding JAM-A/CD321 has gained increasing interest due to its involvement in various diseases, such as cancer, autoimmune disorders, and cardiovascular diseases, where it can influence cell signaling and adhesion mechanisms. Additionally, the functional diversity of JAM-A is highlighted by its interactions with multiple binding partners, including integrins and other adhesion molecules, which modulate cell behavior and fate. The development of recombinant JAM-A proteins facilitates detailed studies of its structure-function relationship, underlying molecular mechanisms, and potential therapeutic applications. Understanding the biological roles of JAM-A/CD321 through recombinant protein studies may offer insights into novel therapeutic strategies targeting inflammatory and metastatic pathways, highlighting its significance in biomedical research and potential clinical interventions.

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