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Brand: ProteoGenix

Nimotuzumab Biosimilar – Anti-EGFR mAb – Research Grade

  • PX-TA1054
Clonality:
Monoclonal Antibody
Isotype:
IgG1, kappa

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Nimotuzumab Biosimilar - Anti-EGFR mAb - Research Grade

Product name Nimotuzumab Biosimilar - Anti-EGFR mAb - Research Grade
Source CAS 828933-51-3   
Species Humanized
Molecular weight 148kDa
Purity >85%
Buffer PBS buffer PH7.5
Delivery condition Blue ice (+4°C)
Delivery Time 3-5 days if in stock; 3-5 weeks if production needed
Storage condition store at -80°C
Brand ProteoGenix
Applications ELISA,WB
Aliases /Synonyms Nimotuzumab,Theraloc,hR3,EGFR,anti-EGFR
Reference PX-TA1054
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody
Product name Nimotuzumab Biosimilar - Anti-EGFR mAb - Research Grade
Source CAS 828933-51-3   
Species Humanized
Expression system Mammalian cells
Molecular weight 148kDa
Purity >85%
Buffer PBS buffer PH7.5
Delivery condition Blue ice (+4°C)
Delivery Time 3-5 days if in stock; 3-5 weeks if production needed
Storage condition store at -80°C
Brand ProteoGenix
Applications ELISA,WB,,,
Aliases /Synonyms Nimotuzumab,Theraloc,hR3,EGFR,anti-EGFR
Reference PX-TA1054
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody

Title: Nimotuzumab Biosimilar: A Promising Anti-EGFR mAb for

Cancer Treatment Introduction:

Nimotuzumab Biosimilar, also known as Anti-EGFR mAb, is a monoclonal antibody that targets the epidermal growth factor receptor (EGFR). It is a biosimilar version of the original Nimotuzumab, which was developed by the Cuban Center for Molecular Immunology and has been approved for the treatment of various types of cancer in over 40 countries. Nimotuzumab Biosimilar has shown promising results in pre-clinical and clinical studies and is currently being researched as a potential therapeutic option for cancer.

Structure:

Nimotuzumab Biosimilar is a humanized IgG1 monoclonal antibody with a molecular weight of approximately 150 kDa. It is composed of two heavy chains and two light chains, each containing a variable region and a constant region. The variable region of the antibody is responsible for binding to the EGFR, while the constant region plays a role in effector functions such as complement activation and antibody-dependent cellular cytotoxicity.

Activity:

Nimotuzumab Biosimilar exerts its anti- cancer activity by binding to the extracellular domain of EGFR, a transmembrane receptor that is overexpressed in many types of cancer. This binding blocks the binding of ligands, such as epidermal growth factor (EGF), to the receptor, thereby inhibiting downstream signaling pathways that promote cell proliferation, survival, and metastasis. In addition, Nimotuzumab Biosimilar can also induce internalization and degradation of EGFR, further reducing its activity.

Application:

Nimotuzumab Biosimilar has been studied in various types of cancer, including head and neck, lung, brain, breast, and colorectal cancer. In pre-clinical studies, it has shown promising results in inhibiting tumor growth and inducing tumor cell death. In clinical trials, it has been found to be well-tolerated and has shown efficacy in combination with chemotherapy or radiotherapy, as well as in monotherapy. It has also been shown to have a favorable safety profile, with minimal side effects compared to other anti-EGFR therapies.

Therapeutic Target:

The EGFR is a well-known therapeutic target in cancer due to its role in promoting tumor growth and progression. Overexpression of EGFR has been observed in various types of cancer, and it has been associated with poor prognosis and resistance to treatment. Therefore, targeting EGFR with Nimotuzumab Biosimilar can potentially lead to improved outcomes for cancer patients.

Conclusion:

Nimotuzumab Biosimilar is a promising anti-EGFR mAb that has shown efficacy in pre-clinical and clinical studies for the treatment of various types of cancer. Its unique mechanism of action and favorable safety profile make it a promising therapeutic option for cancer patients. Further research and clinical trials are needed to fully evaluate its potential in cancer treatment.

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