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Zuberitamab Biosimilar – Anti-MS4A1 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 nameZuberitamab Biosimilar - Anti-MS4A1 mAb - Research Grade
SourceCAS 2251143-19-6
SpeciesChimeric
Purity>85%
BufferPBS buffer PH7.5
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3 week if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsZuberitamab,HS006,IMMUNOGLOBULIN G1, ANTI-(HUMAN CD20 ANTIGEN) (HUMAN-MUS MUSCULUS MONOCLONAL HS006 .GAMMA.1-CHAIN), DISULFIDE WITH HUMAN-MUS MUSCULUS MONOCLONAL HS006 .KAPPA.-CHAIN, DIMER, RHCACD20MA, HS-006,MS4A1,anti-MS4A1
ReferencePX-TA1744
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1,Kappa
ClonalityMonoclonal Antibody

Description of Zuberitamab Biosimilar - Anti-MS4A1 mAb - Research Grade

Introduction

Zuberitamab Biosimilar, also known as Anti-MS4A1 mAb, is a monoclonal antibody that has been developed as a biosimilar to the original Zuberitamab. This biosimilar has been designed to target MS4A1, a protein found on the surface of B-cells. In this article, we will discuss the structure, activity, and potential applications of Zuberitamab Biosimilar as a research-grade antibody.

Structure of Zuberitamab Biosimilar

Zuberitamab Biosimilar is a humanized monoclonal antibody, meaning that it is derived from human cells and has been engineered to have a high affinity for its target. It is composed of two heavy chains and two light chains, joined together by disulfide bonds. The variable regions of the antibody, which are responsible for binding to MS4A1, are located at the tips of the heavy and light chains.

The constant regions of Zuberitamab Biosimilar are responsible for the effector functions of the antibody, such as activating the immune system to destroy target cells. The constant region of the heavy chain is known as the Fc region, and it is responsible for binding to immune cells and activating them. The constant region of the light chain is known as the Fab region, and it is responsible for binding to the target protein, MS4A1.

Activity of Zuberitamab Biosimilar

Zuberitamab Biosimilar specifically targets MS4A1, a protein that is found on the surface of B-cells. This protein is involved in the regulation of B-cell activation and proliferation, making it an ideal therapeutic target for diseases such as B-cell lymphomas and leukemias.

When Zuberitamab Biosimilar binds to MS4A1, it blocks the activation and proliferation of B-cells, leading to their death. This mechanism of action makes Zuberitamab Biosimilar a promising treatment for B-cell malignancies. Additionally, the Fc region of the antibody can also activate immune cells, such as natural killer cells, to further enhance the destruction of target cells.

Applications of Zuberitamab Biosimilar

Zuberitamab Biosimilar is currently being studied for its potential use in the treatment of B-cell malignancies, such as B-cell lymphomas and leukemias. It is being evaluated in clinical trials as a monotherapy and in combination with other treatments, such as chemotherapy and other targeted therapies.

As a research-grade antibody, Zuberitamab Biosimilar can also be used in laboratory settings to study the role of MS4A1 in B-cell function and disease. It can also be used to develop diagnostic tests for B-cell malignancies, as well as to screen potential therapeutic agents that target MS4A1.

Conclusion

Zuberitamab Biosimilar is a humanized monoclonal antibody that specifically targets MS4A1, a protein found on the surface of B-cells. Its unique mechanism of action makes it a promising treatment for B-cell malignancies, and it is currently being studied in clinical trials. As a research-grade antibody, Zuberitamab Biosimilar also has potential applications in laboratory research and diagnostic testing. With further research and development, Zuberitamab Biosimilar has the potential to improve outcomes for patients with B-cell malignancies and advance our understanding of B-cell biology.

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