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Detumomab Biosimilar – Anti-B-cell lymphomas  mAb – Research Grade

Reference:
Size

100ug, 1MG

Isotype

IgG1

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

Mammalian cells

Applications

Elisa, WB

Product nameDetumomab Biosimilar - Anti-B-cell lymphomas  mAb - Research Grade
SourceCAS 145832-33-3
SpeciesMus musculus
Purity>85%
BufferPBS buffer PH7.5
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3-5 weeks if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsDetumomab,SPECIFID(panel of 15 anti-idiotype antibodies),B-cell lymphomas ,anti-B-cell lymphomas 
ReferencePX-TA1225
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1
ClonalityMonoclonal Antibody

Description of Detumomab Biosimilar - Anti-B-cell lymphomas  mAb - Research Grade

Introduction

Detumomab Biosimilar, also known as Anti-B-cell lymphomas mAb, is a monoclonal antibody (mAb) that has been developed as a biosimilar to the original drug, Rituximab. It is a therapeutic agent that specifically targets B-cell lymphomas, a type of cancer that affects the body’s immune system. In this article, we will discuss the structure, activity, and application of Detumomab Biosimilar in detail.

Structure of Detumomab Biosimilar

Detumomab Biosimilar is a recombinant humanized IgG1 monoclonal antibody. It is composed of two heavy chains and two light chains, each containing a variable region and a constant region. The variable regions are responsible for binding to the target antigen, while the constant regions determine the antibody’s effector functions.

The amino acid sequence of Detumomab Biosimilar is highly similar to that of Rituximab, with only a few differences in the constant region. This allows for a similar binding affinity and specificity towards the target antigen, while also reducing the risk of immunogenicity.

Activity of Detumomab Biosimilar

Detumomab Biosimilar works by specifically targeting the CD20 antigen, which is found on the surface of B-cells. Once bound to the CD20 antigen, it triggers a series of events that lead to the destruction of the B-cells.

Firstly, the binding of Detumomab Biosimilar to CD20 activates the complement system, leading to the formation of the membrane attack complex (MAC). The MAC creates pores in the cell membrane, causing the B-cell to burst and die.

Secondly, the binding of Detumomab Biosimilar also activates natural killer (NK) cells, which are part of the body’s immune system. The NK cells then release cytotoxic molecules, such as perforin and granzymes, which directly kill the B-cells.

Lastly, Detumomab Biosimilar can also induce apoptosis (programmed cell death) in B-cells through the activation of the Fas pathway. This mechanism is particularly important in the treatment of B-cell lymphomas, as these cancer cells have a high rate of proliferation and are resistant to apoptosis.

Application of Detumomab Biosimilar

Detumomab Biosimilar is primarily used for the treatment of B-cell lymphomas, including non-Hodgkin’s lymphoma and chronic lymphocytic leukemia. It is also being investigated for its potential in the treatment of other B-cell disorders, such as autoimmune diseases and certain types of solid tumors.

In addition to its therapeutic use, Detumomab Biosimilar is also widely used in research settings. Its high specificity and affinity towards the CD20 antigen make it a valuable tool for studying B-cell biology and the mechanisms of action of other antibodies targeting the same antigen.

Conclusion

Detumomab Biosimilar is a recombinant humanized monoclonal antibody with a similar structure and activity to Rituximab. It specifically targets the CD20 antigen on B-cells and induces their destruction through multiple mechanisms. Its application in the treatment of B-cell lymphomas has shown promising results, and it is also widely used in research settings. With its potential as a biosimilar to Rituximab, Detumomab Biosimilar has the potential to provide an effective and more affordable treatment option for patients with B-cell lymphomas.

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