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Human IL-17A Antibody - Secukinumab Biosimilar

Product Unit size Cat. code Docs. Qty. Price

Anti-hIL17A-hIgG1

Human IL-17A (Secukinumab) antibody - Human IgG1

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100 µg

3 x 100 µg

hil17a-mab1
+-
$109

Anti-human IL-17A - Secukinumab biosimilar - CAS #1229022-83-6

Binding of Anti-hIL-17A-hIgG1 (Secukinumab)
Binding of Anti-hIL-17A Secukinumab

InvivoGen also offers:

HEK-Blue™ IL-17 cells
Recombinant human IL-17A

Anti-hIL-17A-hIgG1 is a biosimilar antibody of Secukinumab, a human interleukin-17A (IL-17A) antibody that specifically blocks IL-17A signaling. This monoclonal antibody (mAb) is FDA-approved for treating moderate-to-severe plaque psoriasis, ankylosing spondylitis, and psoriatic arthritis.

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Anti-hIL-17A-hIgG1 comprises the variable region of Secukinumab and the IgG1 constant region of Secukinumab, mediating high effector functions. 

This antibody can be used together with HEK-Blue™ IL-17 cells for screening and neutralization assays to block IL-17A signaling induced by recombinant human IL-17A (see figure).

 

Key features

  • Each lot is functionally tested and validated.
  • The complete sequence of the antibody construct has been verified.
  • The absence of endotoxins is determined by the EndotoxDetect™ assay.

 

All InvivoGen products are for internal research use only, and not for human or veterinary use.

Figures

Neutralization of IL-17A using Secukinumab biosimilar
Neutralization of IL-17A using Secukinumab biosimilar

Dose-dependent inhibition of HEK-Blue™ IL-17 cell response using Secukinumab biosimilar. Increasing concentrations of Anti-hIL-17-hIgG1 (0.1 ng/ml - 10 µg/ml) were incubated with recombinant human IL-17A (1 ng/ml) for 1 hour prior to the addition of HEK-Blue IL-17 cells. After overnight incubation, SEAP activity in the cell culture supernatant was assessed using QUANTI-Blue™ Solution. Data are shown as the percentage of activity (mean ± SEM).

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Specifications

Application: Neutralization assay, ELISA

Isotype:  Human IgG1, kappa

Recommended isotype control: Human IgG1

Target: Human IL-17A

Species reactivity: Human

Clone: Secukinumab, AIN457, Cosentyx 

Cas number: 1229022-83-6

Source: CHO cells 

Production: Animal-free

Purification: Protein A

Molecular weight: 148 kDa

Physical form: Lyophilized

Formulation buffer: Sodium phosphate buffer with glycine, saccharose, and stabilizing agents

Preservative: Azide-free

Reconstitution buffer: Sterile water (not provided)

Purity: ≥ 95 %

Quality control: Each lot is functionally tested and validated.

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Contents

Anti-hIL-17A-hIgG1 purified monoclonal antibody is provided azide-free and lyophilized. It is available in two quantities:

  • hil17a-mab1: 100 µg
  • hil17a-mab1-03: 3 x 100 µg

store Upon receipt, store lyophilized antibody at -20 °C.

stability The lyophilized product is stable for at least 1 year.

Alert Avoid repeated freeze-thaw cycles.

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Details

Secukinumab background

Secukinumab (AIN457), a fully human anti-hIL-17A-hIgG1 mAb, was designed to selectively target the human interleukin-17A (IL-17A), a pro-inflammatory cytokine involved in Th17 immunity as well as in the pathogenesis of autoimmune diseases [1]. IL-17A, also known as CTLA‑8, is able to induce chemokine production, neutrophil influx, and the production of antibacterial peptides [2].

By binding IL-17A, Secukinumab prevents its interaction with the IL-17 receptor complex (IL-17RA/RC), thereby inhibiting downstream inflammatory signaling and cytokine production [2-3]. Secukinumab has demonstrated strong clinical efficacy in improving skin lesions and joint symptoms. In 2015, this first-in-class anti-IL-17A mAb was approved by the FDA for the treatment of moderate-to-severe plaque psoriasis, leading to the complete clearance of psoriatic plaques [3]. One year later, Secukinumab was also approved for the treatment of ankylosing spondylitis (AS) and psoriatic arthritis (PsA) [3]. Surprisingly, trials of Secukinumab in Crohn’s disease were terminated early due to worsening of the disease in the treatment group [2-3]. These findings agree with IL-17's supportive role in skin wound healing [2].

 

 

References:

1. Monin L. & Gaffen S.L., 2018. Interleukin 17 family cytokines: signaling mechanisms, biological activities, and therapeutic implications. Cold Spring Harb Perspect Biol. 10(4).
2. Huangfu L, Li R, Huang Y, Wang S, 2023. The IL-17 family in diseases: from bench to bedside. Signal Transduct Target Ther.11;8(1):402.
3. Amatya N, Garg AV, Gaffen SL, 2017. IL-17 Signaling: The Yin and the Yang. Trends Immunol. 38(5):310-322

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