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cBR96 Biosimilar – Anti-Lewis Y 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 namecBR96 Biosimilar - Anti-Lewis Y mAb - Research Grade
SpeciesHumanized
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 /SynonymscBR96,cBR96,huAnti-B4,humanized B1-8,humanized D1.3,humanized DX48,humanized K20,humanized-HCMV16,humanized-HCMV37,,Lewis Y,anti-Lewis Y
ReferencePX-TA1108
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1-kappa,
ClonalityMonoclonal Antibody

Description of cBR96 Biosimilar - Anti-Lewis Y mAb - Research Grade

Introduction

The cBR96 biosimilar is a research grade anti-Lewis Y monoclonal antibody (mAb) that has been developed as a potential therapeutic agent for various types of cancer. This biosimilar is a highly specific and potent antibody that targets the Lewis Y antigen, a tumor-associated carbohydrate antigen that is overexpressed in many types of cancer cells. In this article, we will delve into the structure, activity, and potential applications of the cBR96 biosimilar.

Structure of cBR96 Biosimilar

The cBR96 biosimilar is a recombinant humanized IgG1 monoclonal antibody that has been engineered to mimic the structure and function of the original cBR96 antibody. It is composed of two heavy chains and two light chains, each with a variable region that specifically binds to the Lewis Y antigen. The constant regions of the antibody are responsible for its effector functions, such as antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC).

Activity of cBR96 Biosimilar

The primary function of the cBR96 biosimilar is to specifically bind to the Lewis Y antigen, which is overexpressed on the surface of many cancer cells. This binding triggers a series of events that ultimately lead to the destruction of the cancer cells. The cBR96 biosimilar has been shown to induce apoptosis (programmed cell death) in cancer cells, inhibit tumor growth, and enhance the body’s immune response against cancer.

In addition to its direct anti-tumor activity, the cBR96 biosimilar also has the ability to recruit immune cells, such as natural killer (NK) cells and macrophages, to the site of the tumor. These immune cells can then further enhance the destruction of cancer cells through ADCC and CDC mechanisms.

Therapeutic Target: Lewis Y Antigen

The Lewis Y antigen is a carbohydrate antigen that is normally expressed in small amounts on the surface of cells in the body. However, in cancer cells, the expression of this antigen is significantly increased. This makes the Lewis Y antigen an attractive therapeutic target for cancer treatment, as it is highly specific to cancer cells and not found on healthy cells.

The cBR96 biosimilar specifically binds to the Lewis Y antigen, blocking its function and triggering a series of events that lead to the destruction of the cancer cells. This makes it a promising therapeutic option for a wide range of cancers, including breast, lung, ovarian, and prostate cancer.

Research Grade Applications

The cBR96 biosimilar is currently in the research and development phase, with the goal of obtaining regulatory approval for clinical use. As a research grade antibody, it is primarily used in laboratory settings for in vitro and in vivo studies. These studies aim to further understand the mechanism of action of the antibody, determine its efficacy and safety, and explore potential combination therapies.

In addition, the cBR96 biosimilar is also being used in preclinical studies to evaluate its potential for different types of cancer and to optimize dosage and treatment regimens.

Conclusion

In summary, the cBR96 biosimilar is a highly specific and potent anti-Lewis Y monoclonal antibody that has shown promising results in preclinical studies. Its ability to specifically target cancer cells and induce their destruction makes it a promising therapeutic option for a wide range of cancers. As further research and development is conducted, it has the potential to become a valuable addition to the arsenal of cancer treatments.

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