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Rulonilimab Biosimilar – Anti-PD1 mAb – Research Grade

Reference:
Size

100µg, 1MG

Isotype

IgG1, kappa

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa, WB

Product nameRulonilimab Biosimilar - Anti-PD1 mAb - Research Grade
SourceCAS: 2417124-95-7
SpeciesChimeric
BufferPBS buffer PH7.5
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3 week if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsRulonilimab,F-520, F520,PD1,anti-PD1
ReferencePX-TA1761
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1-kappa
ClonalityMonoclonal Antibody

Description of Rulonilimab Biosimilar - Anti-PD1 mAb - Research Grade

Introduction

Rulonilimab is a biosimilar of Anti-PD1 monoclonal antibody (mAb), also known as RUL-1, which is a promising immunotherapy agent targeting the programmed cell death protein 1 (PD-1) pathway. This article will provide a scientific description of the structure, activity, and potential applications of Rulonilimab Biosimilar – Anti-PD1 mAb – Research Grade.

Structure of Rulonilimab Biosimilar

Rulonilimab Biosimilar is a fully humanized IgG4 monoclonal antibody, with a molecular weight of approximately 150 kDa. It is composed of two heavy chains and two light chains, linked by disulfide bonds. The heavy chains consist of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains consist of two constant domains (CL) and one variable domain (VL). The variable domains of both heavy and light chains are responsible for binding to the PD-1 receptor.

Activity of Rulonilimab Biosimilar

Rulonilimab Biosimilar is a potent antagonist of the PD-1 receptor, which is expressed on the surface of T cells, B cells, and natural killer cells. The PD-1 receptor plays a critical role in regulating the immune response by inhibiting T cell activation and proliferation. By binding to the PD-1 receptor, Rulonilimab Biosimilar blocks the interaction between PD-1 and its ligands (PD-L1 and PD-L2), thereby restoring the function of T cells and enhancing the anti-tumor immune response.

In addition to its direct effect on T cells, Rulonilimab Biosimilar also has an indirect effect on other immune cells. It has been shown to increase the secretion of pro-inflammatory cytokines, such as interferon-gamma (IFN-γ) and interleukin-2 (IL-2), by activated T cells. This further enhances the anti-tumor activity of Rulonilimab Biosimilar by promoting the recruitment and activation of other immune cells, such as natural killer cells and macrophages.

Potential Applications of Rulonilimab Biosimilar

Rulonilimab Biosimilar has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of various types of cancer. Its primary therapeutic target is PD-1, which is overexpressed on tumor-infiltrating lymphocytes in many types of cancer, including melanoma, non-small cell lung cancer, and bladder cancer.

In a phase I clinical trial, Rulonilimab Biosimilar demonstrated a favorable safety profile and showed promising anti-tumor activity in patients with advanced solid tumors. In another phase I trial, it showed a durable response in patients with advanced melanoma who had failed previous treatment with anti-PD-1 therapy.

Rulonilimab Biosimilar is also being investigated for its potential in combination therapy with other anti- cancer agents. Preclinical studies have shown that Rulonilimab Biosimilar can enhance the anti-tumor activity of chemotherapy and radiotherapy, making it a promising candidate for combination therapy.

Conclusion

In conclusion, Rulonilimab Biosimilar – Anti-PD1 mAb – Research Grade is a fully humanized monoclonal antibody with a high affinity for PD-1 receptor. It has a potent anti-tumor activity by blocking the PD-1/PD-L1 pathway and promoting the activation of other immune cells. Its potential applications in the treatment of various types of cancer make it a promising candidate for further clinical development.

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