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Eftozanermin Alfa Biosimilar – Anti-TRAILR2 fusion protein – Research Grade

Reference:
Size

100ug, 1MG

Brand

ProteoGenix

Product type

Recombinant Proteins

Expression system

XtenCHO

Applications

Elisa, WB

Product nameEftozanermin Alfa Biosimilar - Anti-TRAILR2 fusion protein - Research Grade
Expression systemXtenCHO
Purity>90% by SDS-PAGE.
Buffer0.01M PBS, pH 7.4.
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3-5 weeks if production needed
Storage condition4°C for short term; -20°C for long term
BrandProteoGenix
Aliases /Synonymsanti-TRAILR2, TRAIL-R2, Death receptor 5, CD262, DR5, Tumor necrosis factor receptor superfamily member 10B, ZTNFR9, TRAIL receptor 2, TRICK2, TNFRSF10B, KILLER, TNF-related apoptosis-inducing ligand receptor 2
ReferencePX-TA2014
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeFusion - [Homo sapiens TNFSF10 (TNF superfamily member 10, tumor necrosis factor (ligand) superfamily, member 10)]2 - Homo sapiens IGHG1 Fc (Fragment constant)

Description of Eftozanermin Alfa Biosimilar - Anti-TRAILR2 fusion protein - Research Grade

Introduction

Eftozanermin Alfa is a biosimilar of the Anti-TRAILR2 fusion protein, a novel therapeutic agent that has shown promising results in preclinical studies. This fusion protein is a potential antibody-based treatment for various diseases, targeting the TRAILR2 protein. In this article, we will provide a comprehensive scientific description of Eftozanermin Alfa, including its structure, activity, and potential applications.

Structure of Eftozanermin Alfa

Eftozanermin Alfa is a fusion protein composed of two parts: the extracellular domain of the TRAILR2 protein and the Fc region of human IgG1. The extracellular domain of TRAILR2 is responsible for binding to its ligand, TRAIL (tumor necrosis factor-related apoptosis-inducing ligand), while the Fc region of IgG1 provides stability and enhances the half-life of the fusion protein.

Activity of Eftozanermin Alfa

Eftozanermin Alfa acts as an antibody against the TRAILR2 protein, which is a member of the tumor necrosis factor (TNF) receptor superfamily. TRAILR2 is expressed on the surface of various cancer cells, making it an attractive therapeutic target. When Eftozanermin Alfa binds to TRAILR2, it induces apoptosis (programmed cell death) in cancer cells, leading to their destruction.

Mechanism of Action

The binding of Eftozanermin Alfa to TRAILR2 triggers the formation of a death-inducing signaling complex (DISC) on the surface of cancer cells. This complex activates the caspase cascade, resulting in the cleavage of various cellular proteins and ultimately leading to cell death. Additionally, Eftozanermin Alfa can also induce cell death through the activation of the intrinsic apoptotic pathway.

Advantages over Other Therapeutic Agents

Eftozanermin Alfa has several advantages over other therapeutic agents currently used for cancer treatment. Unlike chemotherapy, which targets both cancer and healthy cells, Eftozanermin Alfa specifically targets cancer cells, minimizing side effects. Additionally, Eftozanermin Alfa has shown to be effective in various cancer types, including lung, breast, and colon cancer, making it a potential treatment option for a wide range of patients.

Research Grade Eftozanermin Alfa

Research grade Eftozanermin Alfa is a highly purified and characterized form of the fusion protein, specifically designed for use in preclinical studies. It is produced using recombinant DNA technology in mammalian cells, ensuring its high quality and consistency. The use of research grade Eftozanermin Alfa allows for accurate and reliable results in preclinical studies, providing valuable insights into its potential therapeutic applications.

Potential Applications of Eftozanermin Alfa

Eftozanermin Alfa has shown promising results in preclinical studies, making it a potential treatment option for various diseases. Apart from its potential use in cancer treatment, Eftozanermin Alfa has also shown to be effective in other diseases, such as autoimmune disorders and viral infections. Additionally, Eftozanermin Alfa has the potential to be used in combination with other therapies, further enhancing its therapeutic effects.

Conclusion

In summary, Eftozanermin Alfa is a biosimilar of the Anti-TRAILR2 fusion protein, which acts as an antibody against the TRAILR2 protein. Its structure, activity, and potential applications make it a promising therapeutic agent for various diseases, particularly in cancer treatment. Further research and clinical trials are needed to fully understand the potential of Eftozanermin Alfa and its role in improving patient outcomes.

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