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Usilnetug Biosimilar – Anti-AICD-57 mAb – Research Grade

Reference:
Size

100ug, 1MG

Brand

ProteoGenix

Isotype

IgG1, kappa

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa

Product nameUsilnetug Biosimilar - Anti-AICD-57 mAb - Research Grade
SourceCAS: 2770861-19-1
Origin speciesChimeric
Expression systemXtenCHO
Purity>95% by SDS-PAGE.
Buffer0.01M PBS, pH 7.4.
Delivery conditionBlue ice (+4°C)
Delivery lead time in business days3-5 days if in stock; 3-5 weeks if production needed
Storage condition4°C for short term; -20°C for long term
BrandProteoGenix
ReferencePX-TA2146
NoteFor research use only. Not suitable for human use.
IsotypeIgG1-kappa
ClonalityMonoclonal Antibody

Description of Usilnetug Biosimilar - Anti-AICD-57 mAb - Research Grade

Introduction

Usilnetug Biosimilar – Anti-AICD-57 mAb – Research Grade is a novel biosimilar antibody that has been developed for the treatment of autoimmune diseases. This antibody specifically targets the AICD-57 protein, which is a known therapeutic target for various autoimmune disorders. In this article, we will discuss the structure, activity, and application of this biosimilar antibody in detail.

Structure of Usilnetug Biosimilar – Anti-AICD-57 mAb

Usilnetug Biosimilar – Anti-AICD-57 mAb is a monoclonal antibody, which means it is produced from a single clone of immune cells. This antibody is composed of two heavy chains and two light chains, which are connected by disulfide bonds. The heavy chains are approximately 150 kDa in size, while the light chains are about 25 kDa. The overall molecular weight of this antibody is around 200 kDa.

The amino acid sequence of Usilnetug Biosimilar – Anti-AICD-57 mAb is highly similar to the reference product, making it a biosimilar. It has been produced using recombinant DNA technology, where the gene for the antibody was inserted into a host cell, which then produced large quantities of the antibody. This process ensures that the biosimilar antibody has the same structure and function as the reference product.

Activity of Usilnetug Biosimilar – Anti-AICD-57 mAb

Usilnetug Biosimilar – Anti-AICD-57 mAb specifically targets the AICD-57 protein, which is a cell surface receptor that is involved in the regulation of immune responses. This protein is expressed on various immune cells, including T cells, B cells, and natural killer cells. It is known to play a crucial role in the development and progression of autoimmune diseases.

By binding to the AICD-57 protein, Usilnetug Biosimilar – Anti-AICD-57 mAb blocks its activity and modulates the immune response. This helps in reducing inflammation and tissue damage, which are the hallmarks of autoimmune diseases. This antibody has also been shown to induce cell death in AICD-57 expressing cells, providing an additional mechanism of action.

Application of Usilnetug Biosimilar – Anti-AICD-57 mAb

Usilnetug Biosimilar – Anti-AICD-57 mAb is being developed as a potential treatment for various autoimmune diseases, including rheumatoid arthritis, psoriasis, and multiple sclerosis. These diseases are characterized by an overactive immune response, leading to chronic inflammation and tissue damage. By targeting the AICD-57 protein, this biosimilar antibody aims to restore the balance of the immune system and provide relief to patients.

In preclinical studies, Usilnetug Biosimilar – Anti-AICD-57 mAb has shown promising results in reducing disease severity and improving clinical outcomes in animal models of autoimmune diseases. It has also demonstrated a good safety profile, with no significant side effects observed.

Conclusion

In conclusion, Usilnetug Biosimilar – Anti-AICD-57 mAb is a novel biosimilar antibody that specifically targets the AICD-57 protein, a key player in the development of autoimmune diseases. Its structure is similar to the reference product, and it has been produced using recombinant DNA technology. This antibody has shown promising results in preclinical studies and has the potential to be a valuable treatment option for patients with autoimmune diseases. Further clinical trials are needed to establish its efficacy and safety in humans.

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