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Brand: ProteoGenix

Refanezumab Biosimilar – Anti-MAG, SIGLEC-4A mAb – Research Grade

  • PX-TA1411
Clonality:
Monoclonal Antibody
Isotype:
IgG1, kappa

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Refanezumab Biosimilar - Anti-MAG, SIGLEC-4A mAb - Research Grade

Product name Refanezumab Biosimilar - Anti-MAG, SIGLEC-4A mAb - Research Grade
Source CAS 1233953-61-1
Species 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 Refanezumab,GSK-249320,MAG, SIGLEC-4A,anti-MAG, SIGLEC-4A
Reference PX-TA1411
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody
Product name Refanezumab Biosimilar - Anti-MAG, SIGLEC-4A mAb - Research Grade
Source CAS 1233953-61-1
Species Humanized
Expression system Mammalian cells
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 Refanezumab,GSK-249320,MAG, SIGLEC-4A,anti-MAG, SIGLEC-4A
Reference PX-TA1411
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody

Introduction:

Refanezumab Biosimilar, also known as Anti-MAG, SIGLEC-4A mAb, is a monoclonal antibody that specifically targets the myelin-associated glycoprotein (MAG) and the sialic acid-binding immunoglobulin-like lectin 4A (SIGLEC-4A). This biosimilar is a research grade antibody that has been developed for potential therapeutic use in various neurological disorders.

Structure:

Refanezumab Biosimilar is a humanized monoclonal antibody, meaning that it is derived from human cells and has been modified to reduce potential immunogenicity. It is composed of two identical heavy chains and two identical light chains, each containing variable and constant regions. The variable regions of the antibody are responsible for binding to the target molecules, MAG and SIGLEC-4A. The constant regions provide stability and effector functions.

Activity:

Refanezumab Biosimilar binds specifically to both MAG and SIGLEC-4A, which are important proteins involved in maintaining the integrity and function of the myelin sheath in the nervous system. MAG is found on the surface of myelin-producing cells and plays a role in the formation and maintenance of myelin. SIGLEC-4A is found on immune cells and is involved in regulating the immune response in the nervous system.

By binding to these two proteins, Refanezumab Biosimilar inhibits their activity and disrupts the interaction between myelin-producing cells and immune cells. This can lead to a reduction in inflammation and damage to the myelin sheath, which is a characteristic feature of many neurological disorders.

Application:

Refanezumab Biosimilar has potential therapeutic applications in various neurological disorders, including multiple sclerosis, Guillain-Barré syndrome, and chronic inflammatory demyelinating polyneuropathy. These disorders are characterized by damage to the myelin sheath, resulting in neurological symptoms such as muscle weakness, numbness, and difficulty with coordination.

By targeting MAG and SIGLEC-4A, Refanezumab Biosimilar has the potential to slow or even reverse the progression of these disorders by reducing inflammation and promoting repair of the damaged myelin sheath. It could also be used in combination with other therapies to enhance their effectiveness.

Conclusion:

In summary, Refanezumab Biosimilar is a research grade monoclonal antibody that specifically targets MAG and SIGLEC-4A, two proteins involved in maintaining the integrity of the myelin sheath in the nervous system. By inhibiting their activity, this biosimilar has the potential to be used as a therapeutic agent in various neurological disorders. Further research and clinical trials are needed to fully understand the potential of Refanezumab Biosimilar in the treatment of these disorders.

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