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Brand: ProteoGenix

Semorinemab Biosimilar – Anti-MAPT mAb – Research Grade

Clonality:
Monoclonal Antibody
Isotype:
IgG4, Kappa

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Semorinemab Biosimilar - Anti-MAPT mAb - Research Grade

Product name Semorinemab Biosimilar - Anti-MAPT mAb - Research Grade
Source CAS 2159141-27-0
Species Chimeric,Humanized
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 Semorinemab ,RO-7105705,MAPT,anti-MAPT
Reference PX-TA1567
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG4-kappa
Clonality Monoclonal Antibody
Product name Semorinemab Biosimilar - Anti-MAPT mAb - Research Grade
Source CAS 2159141-27-0
Species Chimeric,Humanized
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 Semorinemab ,RO-7105705,MAPT,anti-MAPT
Reference PX-TA1567
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG4-kappa
Clonality Monoclonal Antibody

Introduction to Semorinemab Biosimilar

Semorinemab Biosimilar is a research grade antibody that targets the microtubule-associated protein tau (MAPT), a key player in the development of neurodegenerative diseases such as Alzheimer’s and Parkinson’s. This biosimilar is a promising therapeutic candidate for the treatment of these debilitating conditions.

Structure of Semorinemab Biosimilar

Semorinemab Biosimilar is a monoclonal antibody (mAb) that is designed to mimic the structure and function of the humanized anti-MAPT mAb, Semorinemab. It is a recombinant protein produced in mammalian cells, consisting of two identical heavy chains and two identical light chains. These chains are connected by disulfide bonds and form a Y-shaped structure, with two antigen-binding sites at the tips of the arms.

Activity of Semorinemab Biosimilar

Semorinemab Biosimilar works by binding to MAPT and preventing its aggregation into neurofibrillary tangles, a hallmark of neurodegenerative diseases. This aggregation of MAPT is known to disrupt the normal functioning of neurons and leads to their degeneration. By targeting MAPT, Semorinemab Biosimilar helps to reduce the formation of these tangles and thus slows down the progression of neurodegeneration.

Applications of Semorinemab Biosimilar

Semorinemab Biosimilar has potential applications in the treatment of various neurodegenerative diseases, including Alzheimer’s and Parkinson’s. It has shown promising results in preclinical studies, with the ability to reduce the levels of pathological tau and improve cognitive function in animal models. Additionally, Semorinemab Biosimilar has a good safety profile and has been well-tolerated in clinical trials.

Advantages of Semorinemab Biosimilar

Compared to other therapeutic approaches targeting MAPT, Semorinemab Biosimilar has several advantages. As a biosimilar, it is designed to have a similar structure and function as the humanized anti-MAPT mAb, Semorinemab, making it more effective and less likely to cause adverse reactions. It also has a longer half-life, allowing for less frequent dosing and potentially reducing the burden of treatment for patients.

Future prospects of Semorinemab Biosimilar

Semorinemab Biosimilar is currently in the early stages of clinical development, with ongoing phase I trials. If successful, it has the potential to become a novel treatment option for neurodegenerative diseases, providing hope for patients and their families. Additionally, the biosimilar market is expected to grow significantly in the coming years, making Semorinemab Biosimilar a valuable asset for both patients and the pharmaceutical industry.

Conclusion

In summary, Semorinemab Biosimilar is a research grade antibody that targets the microtubule-associated protein tau and has potential applications in the treatment of neurodegenerative diseases. Its structure, activity, and advantages make it a promising therapeutic candidate, with ongoing clinical trials and future prospects for patients and the pharmaceutical industry.

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