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Lomvastomig Biosimilar – Anti-PD1 and TIM3 mAb – Research Grade

Reference:
Size

100ug, 1MG

Isotype

IgG1, kappa

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa, WB

Product nameLomvastomig Biosimilar - Anti-PD1 and TIM3 mAb - Research Grade
SpeciesHomo sapiens
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-PD1, Programmed cell death protein 1, Protein PD-1, hPD-1, PDCD1, CD279, TIM-3, TIM3, hepatitis A virus cellular receptor 2, HAVCR2
ReferencePX-TA2075
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1-kappa
ClonalityMonoclonal Antibody

Description of Lomvastomig Biosimilar - Anti-PD1 and TIM3 mAb - Research Grade

Introduction

Lomvastomig Biosimilar – Anti-PD1 and TIM3 mAb – Research Grade is a novel therapeutic antibody that has shown promising results in the treatment of cancer. This biosimilar is designed to target two important immune checkpoint proteins, PD-1 and TIM-3, which play a crucial role in suppressing the immune response against cancer cells. In this article, we will discuss the structure, activity, and potential applications of this biosimilar in the field of cancer therapy.

Structure of Lomvastomig Biosimilar

Lomvastomig Biosimilar is a monoclonal antibody (mAb) that is produced using recombinant DNA technology. It is a fully humanized antibody, meaning that it is derived from human genes and has a high affinity for its target proteins. The antibody has a Y-shaped structure, with two identical heavy chains and two identical light chains. The heavy chains are composed of constant and variable regions, while the light chains consist of only variable regions. The variable regions of the antibody are responsible for binding to the target proteins, PD-1 and TIM-3.

Activity of Lomvastomig Biosimilar

Lomvastomig Biosimilar works by blocking the interaction between PD-1 and its ligands, PD-L1 and PD-L2, and between TIM-3 and its ligand, galectin-9. These interactions are known to inhibit the activation of T cells, which are the key players in the immune response against cancer cells. By blocking these interactions, Lomvastomig Biosimilar allows the T cells to recognize and attack cancer cells, leading to their destruction. This mechanism of action makes Lomvastomig Biosimilar a potent immunotherapy for cancer treatment.

Therapeutic Target: PD-1 and TIM-3

PD-1 and TIM-3 are immune checkpoint proteins that are expressed on the surface of T cells. These proteins play a crucial role in regulating the immune response by preventing the overactivation of T cells. However, cancer cells can exploit this mechanism to evade the immune system and continue to grow and spread. This is where Lomvastomig Biosimilar comes in, by targeting these proteins and blocking their inhibitory effects, it allows the immune system to mount a strong response against cancer cells.

Application of Lomvastomig Biosimilar

Lomvastomig Biosimilar has shown promising results in the treatment of various types of cancer, including melanoma, non-small cell lung cancer, and renal cell carcinoma. It is currently being evaluated in clinical trials, and early results have shown significant improvement in patient outcomes. In addition to its use as a monotherapy, Lomvastomig Biosimilar can also be combined with other cancer treatments, such as chemotherapy and radiation therapy, to enhance their effectiveness.

Conclusion

In conclusion, Lomvastomig Biosimilar – Anti-PD1 and TIM3 mAb – Research Grade is a novel therapeutic antibody that targets two important immune checkpoint proteins, PD-1 and TIM-3. Its structure, activity, and potential applications make it a promising candidate for the treatment of various types of cancer. As further research and clinical trials continue, Lomvastomig Biosimilar has the potential to revolutionize the field of cancer therapy and improve patient outcomes.

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