Recombinant human IL-13
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Cat.code:
rcyc-hil13NEW
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ABOUT
Human IL-13 protein - Mammalian cell-expressed, tag-free, carrier-free
Recombinant human IL-13 is a high-quality and biologically active cytokine, validated using proprietary IL-4/IL-13 reporter cells. This member of the IL-2/γc superfamily is produced in CHO cells to ensure protein glycosylation and bona fide 3D structure.
Recombinant human IL-13 can be used together with HEK-Blue™ IL-4/IL-13 cells for the screening of inhibitory molecules, such as Dupilumab, a therapeutic monoclonal antibody targeting the IL-4Rα subunit of the IL-13 receptor (see figures).
Key features
- Each lot is validated using HEK-Blue™ IL-4/IL-13 cells
- Endotoxin ≤ 0.1 EU/µg
- 0.2 µm sterile-filtered
Applications
- Standard for IL-13 detection and quantification
- Screening and release assays for antibodies blocking IL-13 signaling
- Screening and release assays for engineered IL-13
Interleukin 13 (IL-13) shares a common receptor subunit, IL-4Rα, with IL-4. These two cytokines play an important role in anti-parasitic immune responses. Dysregulated IL-4 /IL-13 expression contributes to Th2-mediated diseases, including asthma and atopic dermatitis.
All InvivoGen products are for internal research use only, and not for human or veterinary use.
SPECIFICATIONS
Specifications
P35225 (with mutation Q144R)
100 μg/ml in water
Phosphate buffer saline (pH 7.4), 5% saccharose
0.2 µm filtration
The absence of bacterial contamination (e.g. lipoproteins and endotoxins) has been confirmed using HEK-Blue™ TLR2 and HEK‑Blue™ TLR4 cells.
Cellular assays (tested), ELISA
Each lot is functionally tested and validated.
CONTENTS
Contents
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Product:Recombinant human IL-13
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Cat code:rcyc-hil13
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Quantity:10 µg
1.5 ml endotoxin-free water
Shipping & Storage
- Shipping method: Room temperature
- -20°C
- Avoid repeated freeze-thaw cycles
Storage:
Caution:
Details
Interleukin 13 background
IL-13 is a cytokine that belongs to the IL-2/γc superfamily. IL-13 is produced as a secreted monomeric molecule by activated CD4+ T cells, Natural Killer T cells (NKT cells), group 2 innate lymphoid cells (ILC2s), macrophages, mast cells, basophils, or eosinophils [1].
IL-13 binds a heterodimeric receptor composed of the IL-4Rα and IL-13Rα1 chains. This receptor is shared with IL-4, which can bind two different receptors: Type I (IL-4Rα and common γ chain) and Type II (IL-4Rα and IL-13Rα1). The binding of IL-13 to its receptor triggers a signaling cascade leading to the activation of STAT6. Subsequent gene expression drives M2 macrophage polarization, B-cell proliferation, IgE immunoglobulin class switching, and eosinophil activation and survival [1]. In non-hematopoietic cells, IL-13 is essential for mucus production, goblet cell hyperplasia, and worm expulsion [1]. Altogether, the downstream IL-13 effector functions participate in parasitic infection clearance and allergic reactions [1].
Relevance for therapeutics development
IL-13 is a key cytokine for controlling infections by extracellular parasites. However, along with IL-4, it also contributes to harmful allergic responses [1, 2]. As the prevalence of chronic allergic diseases such as asthma and atopic dermatitis is increasing worldwide, there has been a keen interest in the therapeutic blocking of IL-4 and IL-13 signaling.
Dupilumab is a fully human monoclonal antibody (mAb) that targets the IL-4Rα subunit [3]. It acts like a receptor antagonist and inhibits the signaling of both IL-4 and IL-13 [3]. Dupilimab was FDA-approved in 2017 for treating asthma, atopic dermatitis, and chronic sinusitis [3, 4]. Due to its favorable safety profile and established clinical use, Dupilumab holds significant promise for amending treatment options for many dermatologic conditions [5].
Tralokinumab and Lebrikizumab are fully human mAbs that target IL-13, inhibiting its receptor binding ability. Tralokinumab and Lebrikizumab were FDA-approved in 2021 and 2024, respectively, for treating moderate-to-severe atopic dermatitis [6, 7]
References:
1. Bernstein, Z.J., et al., 2023. Engineering the IL-4/IL-13 axis for targeted immune modulation. Immunol Rev. 320(1):29-57.
2. Ogulur, I., et al., 2025. Type 2 immunity in allergic diseases. Cell & Mol Immunol, 22(3):211-242.
3. Harb, H. & Chatila, T.A., 2020. Mechanisms of Dupilumab. Clin Exp Allergy. 50(1):5-14.
4. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/761055s040lbl.pdf
5. Olbrich, H., et al., 2023. Dupilumab in Inflammatory Skin Diseases: A Systematic Review. Biomolecules.13(4):634.
6. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2022/761180Orig1s000lbl.pdf
7. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/761306Orig1s000correctedlbl.pdf
DOCUMENTS
Documents
Technical Data Sheet
Validation Data Sheet
Safety Data Sheet
Certificate of analysis
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