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Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb – Research Grade

Reference:
Size

100ug, 1MG

Isotype

IgG1-lambda/kappa

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa, WB

Product nameForimtamig Biosimilar - Anti-GPRC5D and CD3 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-GPRC5D, CD3
ReferencePX-TA2067
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1-lambda/kappa
ClonalityMonoclonal Antibody

Description of Forimtamig Biosimilar - Anti-GPRC5D and CD3 mAb - Research Grade

Introduction

Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb is a novel therapeutic antibody that has shown promising results in preclinical studies. This biosimilar is designed to target two key proteins, GPRC5D and CD3, which are involved in the development and progression of various cancers. In this article, we will provide a detailed description of the structure, activity, and potential applications of this biosimilar.

Structure of Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb

Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb is a monoclonal antibody (mAb) that is produced through recombinant DNA technology. It is composed of two identical heavy chains and two identical light chains, each containing a variable region and a constant region. The variable regions of the antibody are responsible for binding to GPRC5D and CD3, while the constant regions provide stability and effector functions.

The mAb has a molecular weight of approximately 150 kDa and is glycosylated, meaning it has sugar molecules attached to it. This glycosylation is important for the stability and function of the antibody.

Activity of Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb

The primary activity of Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb is to target and bind to two specific proteins, GPRC5D and CD3. GPRC5D is a cell surface receptor that is overexpressed in multiple myeloma and other hematological malignancies. CD3 is a protein found on the surface of T cells, which are key players in the immune response against cancer cells.

By binding to GPRC5D and CD3, this biosimilar can mediate a dual mechanism of action. First, it can directly kill cancer cells by inducing cell death through various pathways. Second, it can activate T cells and enhance their ability to recognize and attack cancer cells. This dual mechanism of action makes Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb a potentially powerful therapeutic agent for the treatment of cancer.

Potential Applications of Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb

The primary application of Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb is in the treatment of multiple myeloma and other hematological malignancies. Preclinical studies have shown that this biosimilar can effectively kill cancer cells and inhibit tumor growth in animal models of multiple myeloma and other blood cancers.

In addition to its potential as a standalone therapy, Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb can also be used in combination with other treatments, such as chemotherapy and immunotherapy, to enhance their efficacy. Furthermore, this biosimilar can also be used in the research setting to study the role of GPRC5D and CD3 in cancer development and to develop new therapies targeting these proteins.

Conclusion

Forimtamig Biosimilar – Anti-GPRC5D and CD3 mAb is a promising therapeutic antibody that targets two key proteins involved in the development and progression of cancer. Its unique dual mechanism of action and potential applications make it a valuable addition to the arsenal of cancer treatments. Further clinical studies are needed to fully evaluate the efficacy and safety of this biosimilar, but early results are promising and warrant further investigation.

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