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IL23R

Products

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All listed services and products are For Research Use Only. Do Not use in any diagnostic or therapeutic applications.

Background

IL23R is a type I transmembrane glycoprotein belonging to the class I cytokine receptor superfamily, with the full-length core polypeptide having an estimated molecular weight of approximately 70 kDa that can increase after N-linked glycosylation. This receptor heterodimerizes with IL12Rβ1 to form an active receptor complex on the surface of Th17 cells, innate lymphoid cells, macrophages, dendritic cells, and activated natural killer cells. IL-23 is a heterodimeric cytokine composed of a unique p19 subunit and the common p40 subunit shared with IL-12 that engages this receptor complex. IL23R ligation activates the receptor-associated kinases JAK2 and TYK2, leading to phosphorylation of receptor-associated signaling components and downstream STAT proteins. STAT3 is a major mediator of IL-23 signaling, with STAT4 also contributing in a cell-type-dependent manner. Activated STAT3 and STAT4 translocate to the nucleus and regulate transcriptional programs that promote the expression of effector molecules including IL-17A, IL-17F, IL-22, and granulocyte-macrophage colony-stimulating factor (GM-CSF).

Fig.1 IL23R pathway. (OA Literature)Fig.1 Signaling by IL-23R.1

IL23R Protein Function: A Central Node in the IL-23/Th17 Inflammatory Axis

IL23R biological function permeates several interconnecting physiological and pathological networks:

  • Th17 Cell Differentiation and Maintenance: Naive CD4+ T cells require IL-6 in combination with TGF-β in vitro to differentiate into the pathologic Th17 type cell lineage; however, for this process to be completed along with stabilization this must occur through signaling via IL23R. Recognition of IL23R results in blocking apoptosis of Th17 cells and sustained discovery of producing effector functions that enable continued secretion of pro-inflammatory cytokines, including IL-17, that can drive tissue damage from autoimmune settings.

Psoriasis and Cutaneous Inflammation: The IL-23/IL-17 axis is currently recognized as a major pathway involved in plaque psoriasis pathogenesis. Experimental intradermal injection of IL-23 in wild-type mice induces epidermal hyperplasia, erythema, and inflammatory infiltrates that resemble key features of human psoriatic lesions.

  • Inflammatory Bowel Disease: IL-23 signalling in the intestinal mucosa promotes pathogenic T-cell responses and activates innate lymphoid cells that support chronic inflammation in Crohn's Disease and ulcerative colitis.

IL23R Membrane Protein Product

Advance your cytokine receptor research with our recombinant IL23R protein offerings for autoimmune disease research. The type I transmembrane topology, extensive disulfide bonding, and glycosylation-dependent folding of IL23R present particular production challenges. With these considerations in mind, appropriate expression and formulation strategies can be selected to produce IL23R constructs suitable for different research applications. Available research formats may include membrane-associated receptor constructs and soluble extracellular domain (ECD) proteins, while receptor complex formats can be evaluated according to specific product availability and project requirements. Expression systems, construct design, and characterization strategies are selected according to the intended protein format and application. These preparations can be characterized using appropriate biochemical and biophysical methods to support structural studies, ligand-binding assays, and antibody screening.

IL23R Protein Product

Not finding the membrane protein product you need? Contact us to start your one-stop custom service!

IL23R Stable Cell Line Product

Development of reliable, reproducible cellular models unequivocally dissecting IL23R-driven biology is important for testing therapeutic candidates. We have cationic stable cassette generating methods for the co-expression of wild-type or disease-related human, mouse and rat IL23R forms alongside a symmetrical loss-of-function modulated endogenous expression assay. They are additionally amenable to use with high-throughput IL-23 neutralization assays, Th17 differentiation studies, STAT3 reporter gene analysis and cytokine profiling thus providing the experimental reproducibility requisite for multi-phase research priorities in parallel.

IL23R Stable Cell Line Product

Not finding the stable cell line product you need? Contact us to start your one-stop custom service!

IL23R Recombinant Antibody Product

Our comprehensive portfolio includes high-affinity recombinant antibodies against IL23R developed to our high standards for any of your research needs. Compared with traditional polyclonal antibodies, these next-generation recombinant-derived monoclonal antibodies exhibit superior specificity, sensitivity and batch-to-batch consistency. Each of our IL23R recombinant antibodies is validated for WB/ ELISA/ FCM/ IF/ ICC/ IHC (mouse, rat, monkey), specificity detection in various samples (such as T-cell lysates, tissue section from psoriatic plaques and intestinal biopsies).

IL23R Recombinant Antibody Product

Not finding the recombinant antibody product you need? Contact us to start your one-stop custom service!

Product Features

  • High Purity & Activity: High purity and verified integrity for dependable downstream work.
  • Diverse Expression Systems: Choice of expression formats to match routine or specialized projects.
  • Species Reactivity: Products available for human, mouse, pig, and other species.
  • Validated Applications: Application-tested to deliver consistent signals across common lab workflows.
  • Exceptional Lot-to-Lot Consistency: Tight lot-to-lot control for reproducible performance.
  • Customization Options: Flexible customization of tags, labels, or packaging upon request.

Custom IL23R Membrane Protein and Antibody Discovery Services

In addition to our catalogue products, we supply custom services for your membrane protein and antibody discovery and development needs. Drawing upon our deep knowledge of cytokine receptor biology and autoimmune disease pharmacology, we can help you with:

  • Custom IL23R Receptor Production: Tailored expression, purification, and characterization of challenging multi-domain receptor constructs.
  • Custom Antibody Development: From antigen design to antibody engineering (monoclonal, polyclonal, recombinant) for specific research applications.
  • Stable Cell Line Development: Generation of bespoke stable cell lines expressing your target of interest.
  • Functional Assay Development: Designing and executing assays to assess receptor activation and ligand.

Frequently Asked Questions (FAQ)

  1. Do you sell IL23R products as clinical use or diagnostic use?

    No, IL23R products and services are offered for research purposes only, not intended for clinical diagnosis, prevention, treatment or cure of any disease.

  2. Do you find stable cell lines that inducibly express or co-express IL23R with IL12RB1?

    Absolutely. Our cell engineering team routinely generates tetracycline-inducible systems and lines co-expressing IL23R with IL12RB1, JAK2, TYK2, or STAT3 reporter constructs for comprehensive pathway analysis. We welcome detailed discussions regarding your preferred expression architecture and phenotypic requirements.

  3. What species variants are available?

    Our catalog includes human, mouse, and rat IL23R reagents. Custom production of additional orthologs or engineered mutants—including the protective R381Q variant, JAK2-binding deficient mutants, and domain-specific truncations—can be arranged upon request.

  4. What types of IL23R products do you offer?

    We offer a range of products including recombinant full-length IL23R, soluble extracellular domain (exIL-23R), IL23R-IL12RB1 heterodimeric complexes, stable cell lines expressing IL23R or its signaling components, and high-quality recombinant IL23R antibodies, along with comprehensive custom services.

Reference
  1. Audia, Salvatore, et al. "The IL-23R and its genetic variants: A hitherto unforeseen bridge between the immune system and cancer development." Cancers 17.1 (2024): 55. Under Open Access license CC BY 4.0, without modification. https://doi.org/10.3390/cancers17010055
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