Recombinant human IL-29 (IFN-λ1) protein - Bioactive cytokine

Recombinant cytokine, source: CHO cells

SPECIFICATIONS

Specifications

Source
CHO cells
Species
Human
Synonyms
Interferon lambda-1
IFNλ1
IFNL1
IL29
Accession sequence

 Q8IU54

Protein size
181 a.a. (G20-T200)
Molecular weight
~25 kDa (SDS-PAGE)
Carrier
Carrier-free
Tag
Tag-free
Purity
≥ 95% (SDS-PAGE)
Solubility

100 μg/ml in water

Formulation buffer

Phosphate buffer saline (pH 7.4), 5% saccharose

Appearance (form)
Lyophilized
Reconstitution buffer
Endotoxin-free water (provided)
Sterility

0.2 µm filtration

Endotoxin

The absence of bacterial contamination (e.g. lipoproteins and endotoxins) has been confirmed using HEK-Blue™ TLR2 and HEK‑Blue™ TLR4 cells.

Applications

Cellular assays (tested)

ELISA

Quality control

Each lot is functionally tested and validated.

CONTENTS

Contents

  • Product: 
    Recombinant human IL-29
  • Cat code: 
    rcyc-hil29
  • Quantity: 
    20 µg
Includes:

1.5 ml endotoxin-free water

Shipping & Storage

  • Shipping method:  Room temperature
  • Storage:

    • -20 °C
    Stability: -20°C for up to 1 year

    Caution:

    • Avoid repeated freeze-thaw cycles

Details

Interleukin-29 (IL-29), also known as interferon lambda 1 (IFNλ1), is one member of the type III IFN family. Together with IFN-λ2 (IL-28a), IFN-λ3 (IL-28b), and IFN-λ4, it plays a pivotal role in mucosal immunity at epithelial barriers, enhancing antiviral immunity and regulating inflammation1. 

When a viral infection is sensed by pattern recognition receptors, IFN-λs are produced by a variety of cell types, predominantly plasma cell-like dendritic cells (DCs). However, the target cell populations of IFN-λ are tissue-restricted and mainly include epithelial cells, DCs, and T cells2. IL-29 binds to a receptor complex composed of IL-28R1 and IL-10R2. The induced JAK-STAT pathway leads to the activation of STAT1 and STAT2, and subsequently combines with IRF9 to form the ISGF3 transcription factor complex2.  Similarly, the activating signaling can also be transmitted to the nucleus via mitogen‐activated protein kinase (MAPK), protein kinase B (Akt), nuclear factor‐kappa B (NF‐κB), and nuclear factor of activated T cell 1 (NFATc1) pathways2.

Besides its antiviral function, IFN-λ signaling also plays an important role in non-infectious diseases like autoimmune diseases and cancer1-2. Increased levels of IL‐29 were detected in the serum of patients with rheumatoid arthritis, psoriasis, as well as systemic sclerosis2. On the other hand, IFN-λ demonstrates broad-spectrum inhibitory activity across cancers, including bladder cancer, melanoma, colorectal carcinoma, and HPV-associated cervical malignancies1. Further research is required to elucidate the dual role of IFN-λ and to gain a deeper understanding of its complex role in immune regulation.

 

1. Tang B, et al., 2025. IFN-λ: Unleashing Its Potential in Disease Therapies From Acute Inflammation Regulation to Cancer Immunotherapy. Immunology. 176(2):197-214. 
2. Wang JM, et al., 2019. Insights into IL-29: Emerging role in inflammatory autoimmune diseases. J Cell Mol Med. 23(12):7926-7932

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