Basic Information
Clone | Cemiplimab Biosimilar |
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Molecular Weight | 150 kDa |
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Endotoxin | <1EU/mg (<0.001EU/μg)Determined by LAL gel clotting assay |
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Sterility | 0.2 μm filtration |
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Aggregation | <5% Determined by SECP |
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Purity | >95% Determined by SDS-PAGE |
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Product Information
Production | Purified from cell culture supernatant in an animal-free facility |
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Purification | Protein A or G purification |
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Storage | 2 - 8°C for up to 4 weeks and -80°C for long term storage (Avoid repeated freezing and thawing) |
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Target Background
Cemiplimab Biosimilar uses the same protein sequences as the therapeutic antibody cemiplimab.PD-L1 and PD-L2 (B2-DC or CD273, programmed cell death ligand 2) are the two ligands for the receptor PD-1 (CD279, programmed cell death protein 1).Cemiplimab (anti-PD-1) is an intravenous human monoclonal antibody directed against programmed cell death-1 receptor (PD-1) and blocks its interaction with programmed death ligands 1 (PD-L1) and 2 (PD-L2). Cemiplimab blocks T-cell inactivation and enhances the immune system's anti-tumor response.Binding of the programmed death receptor (PD) ligands PD-L1 and PD-L2, to the PD-1 receptor inhibits T-cell proliferation and cytokine production. The upregulation of PD-1 ligands occurs in some tumors and signaling through this pathway may contribute to the inhibition of active T-cell immune surveillance of tumors. Cemiplimab is a recombinant human immunoglobulin G4 (IgG4) monoclonal antibody that binds to the PD-1 receptor and blocks its interaction with PD-L1 and PD-L2 ligands, causing PD-1 pathway-mediated inhibition of the immune response, including the anti-tumor immune response. In mouse tumor models, blocking PD-1 activity resulted in decreased rates of tumor growth.
Immunogen Information
Isotype | human IgG4 kappa |
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Immunogen | Human PD-1 |
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RecommendedIsotype Control(s) | In Vivo Grade Recombinant Human IgG4-S228P Kappa Isotype Control Antibody |
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Recommended Dilution Buffer | 1×PBS pH 7.0 |
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* For research use only. Not for therapeutic or diagnostic purposes.