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Mosunetuzumab Biosimilar – Anti-CD3E, MS4A1, CD20 mAb – Research Grade

Reference:
Size

100ug, 1MG

Isotype

IgG1, kappa

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

Mammalian cells

Applications

Elisa, WB

Product nameMosunetuzumab Biosimilar - Anti-CD3E, MS4A1, CD20 mAb - Research Grade
SourceCAS 1905409-39-3
SpeciesHumanized
Expression systemMammalian cells
Purity>85%
BufferPBS buffer PH7.5
Delivery conditionBlue ice (+4°C)
Delivery lead time in business days3-5 days if in stock; 3-5 weeks if production needed
Delivery Time3-5 days if in stock; 3-5 weeks if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsMosunetuzumab,BTCT4465A,RG-7828,RO7030816,CD3E, MS4A1, CD20,anti-CD3E, MS4A1, CD20
ReferencePX-TA1482
NoteFor research use only. Not suitable for human use.
IsotypeIgG1-kappa

Description of Mosunetuzumab Biosimilar - Anti-CD3E, MS4A1, CD20 mAb - Research Grade

The Structure of Mosunetuzumab Biosimilar

Mosunetuzumab Biosimilar is a monoclonal antibody (mAb) that specifically targets three proteins – CD3E, MS4A1, and CD20. It is a biosimilar version of the original Mosunetuzumab, which was developed by Genentech and is currently in clinical trials for the treatment of non-Hodgkin’s lymphoma. The biosimilar version is being developed by a different pharmaceutical company and is intended for research purposes only.

The structure of Mosunetuzumab Biosimilar is similar to that of the original Mosunetuzumab, with a few minor differences. It is a humanized IgG1 antibody, meaning that it is derived from human antibodies and has been modified to reduce immunogenicity. It consists of two heavy chains and two light chains, each containing a variable region and a constant region. The variable region is responsible for binding to the target proteins, while the constant region is responsible for effector functions such as antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC).

The Activity of Mosunetuzumab Biosimilar

Mosunetuzumab Biosimilar is a bispecific antibody, meaning that it can bind to two different proteins at the same time. It binds to CD3E on T cells and MS4A1 on B cells, bringing these two cell types into close proximity. This leads to the activation of T cells, which then release cytokines and other molecules that help to kill the targeted B cells. In addition, Mosunetuzumab Biosimilar also binds to CD20 on B cells, triggering their death through ADCC and CDC.

The ability of Mosunetuzumab Biosimilar to target multiple proteins and activate different immune mechanisms makes it a promising therapeutic option for the treatment of various B cell malignancies. It has shown particularly promising results in the treatment of non-Hodgkin’s lymphoma, where it has demonstrated high response rates in clinical trials.

The Application of Mosunetuzumab Biosimilar

Mosunetuzumab Biosimilar is currently being developed for research purposes only and is not yet approved for clinical use. However, it has the potential to be used as a therapeutic agent for the treatment of various B cell malignancies, including non-Hodgkin’s lymphoma, chronic lymphocytic leukemia, and multiple myeloma.

In addition to its potential as a monotherapy, Mosunetuzumab Biosimilar also has the potential to be used in combination with other therapies, such as chemotherapy or other targeted therapies. Its bispecific nature and ability to activate different immune mechanisms make it a promising candidate for combination therapy, as it can potentially enhance the efficacy of other treatments.

Overall, Mosunetuzumab Biosimilar has shown great promise as a potential therapeutic option for the treatment of B cell malignancies. Its unique structure, targeting multiple proteins, and ability to activate different immune mechanisms make it a versatile and potentially effective treatment option. Further research and clinical trials will be needed to fully understand its potential and determine its safety and efficacy in treating these diseases.

Publication

Joshua S. Bray, Gethin R. Thomas, Victoria M. Smith, Sandrine Jayne, Martin J.S. Dyer, Harriet S. Walter, Comparative in-Vitro Efficacy of CD20xCD3 IgG Bispecific Biosimilar Constructs Against Diffuse Large B Cell Lymphoma (DLBCL) Cell Lines with Different Levels of Expression of CD20,Blood, Volume 144, Supplement 1, 2024, Page 5826, ISSN 0006-4971, https://doi.org/10.1182/blood-2024-203884.

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