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Brand: ProteoGenix

Traxivitug Biosimilar – Anti-Major capsid protein VP1 mAb – Research Grade

Clonality:
Monoclonal Antibody
Isotype:
IgG1-lambda2

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Traxivitug Biosimilar - Anti-Major capsid protein VP1 mAb - Research Grade

Product name Traxivitug Biosimilar - Anti-Major capsid protein VP1 mAb - Research Grade
Source CAS: 2770852-89-4
Origin species Homo sapiens
Expression system XtenCHO
Purity >95% by SDS-PAGE.
Buffer 0.01M PBS, pH 7.4.
Delivery condition Blue ice (+4°C)
Delivery lead time in business days 3-5 days if in stock; 3-5 weeks if production needed
Storage condition 4°C for short term; -20°C for long term
Brand ProteoGenix
Reference PX-TA2143
Note For research use only. Not suitable for human use.
Isotype IgG1-lambda2
Clonality Monoclonal Antibody

Introduction

Traxivitug Biosimilar – Anti-Major capsid protein VP1 mAb – Research Grade, is a novel biosimilar antibody developed for targeting the major capsid protein VP1, a key component of the human polyomavirus JC (JCV). This biosimilar has been designed to mimic the activity of the original monoclonal antibody (mAb) Traxivitug, which has shown promising results in clinical trials for the treatment of progressive multifocal leukoencephalopathy (PML). In this article, we will explore the structure, activity, and potential applications of Traxivitug Biosimilar in the field of immunotherapy.

Structure of Traxivitug Biosimilar

Traxivitug Biosimilar is a recombinant humanized IgG1 monoclonal antibody, with a molecular weight of approximately 150 kDa. It is composed of two heavy chains and two light chains, which are connected by disulfide bonds. The variable regions of the antibody are derived from the original Traxivitug mAb, while the constant regions have been modified to reduce immunogenicity and enhance stability. The specific targeting of the major capsid protein VP1 is achieved through the complementarity-determining regions (CDRs) present in the variable regions of the antibody.

Activity of Traxivitug Biosimilar

The main activity of Traxivitug Biosimilar is its ability to bind to the major capsid protein VP1 of JCV. This binding inhibits the interaction of the virus with its cellular receptor, leading to a decrease in viral entry and replication. Additionally, Traxivitug Biosimilar also triggers an immune response against the virus, further aiding in the clearance of JCV-infected cells. This dual mechanism of action makes Traxivitug Biosimilar a potent therapeutic agent for the treatment of PML.

Potential Applications of Traxivitug Biosimilar

PML is a rare and often fatal brain infection caused by the reactivation of JCV in immunocompromised individuals. Currently, there is no effective treatment for PML, and the mortality rate is high. Traxivitug Biosimilar has the potential to fill this treatment gap and provide a much-needed therapeutic option for patients with PML. In addition, Traxivitug Biosimilar can also be explored for the treatment of other JCV-related diseases, such as progressive multifocal leukoencephalopathy-immune reconstitution inflammatory syndrome (PML-IRIS).

Advantages of Traxivitug Biosimilar

One of the major advantages of Traxivitug Biosimilar is its biosimilarity to the original Traxivitug mAb. This means that it has been extensively characterized and proven to have similar efficacy and safety profile as the original mAb. This reduces the time and cost of development, making Traxivitug Biosimilar a more affordable option for patients. Additionally, as a biosimilar, Traxivitug Biosimilar has the potential to increase access to treatment for patients in need, especially in developing countries.

Conclusion

Traxivitug Biosimilar – Anti-Major capsid protein VP1 mAb – Research Grade, is a promising biosimilar antibody that has the potential to revolutionize the treatment of PML and other JCV-related diseases. Its unique structure, potent activity, and potential applications make it a valuable addition to the field of immunotherapy. Further clinical trials are needed to fully evaluate the safety and efficacy of Traxivitug Biosimilar, but the initial results are promising and offer hope for patients suffering from PML.

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