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Apitegromab Biosimilar – Anti-pro-GDF-8 mAb – Research Grade

Reference:
Size

100µg, 1MG

Isotype

IgG4-lambda

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa, WB

Product nameApitegromab Biosimilar - Anti-pro-GDF-8 mAb - Research Grade
SpeciesHomo Sapiens
Expression systemXtenCHO
BufferPBS buffer PH7.5
Delivery conditionBlue ice (+4°C)
Delivery lead time in business days3-5 days if in stock; 3-5 weeks if production needed
Delivery Time3-5 days if in stock; 3 week if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsApitegromab,,pro-GDF-8,anti-pro-GDF-8
ReferencePX-TA1810
NoteFor research use only. Not suitable for human use.
IsotypeIgG4 Lambda
ClonalityMonoclonal Antibody

Description of Apitegromab Biosimilar - Anti-pro-GDF-8 mAb - Research Grade

Introduction to Apitegromab Biosimilar – Anti-pro-GDF-8 mAb – Research Grade

Apitegromab Biosimilar, also known as Anti-pro-GDF-8 monoclonal antibody (mAb), is a research grade therapeutic antibody that is designed to target and inhibit the activity of growth differentiation factor 8 (GDF-8). GDF-8 is a protein that belongs to the transforming growth factor beta (TGF-β) superfamily and is involved in regulating muscle growth and development.

Structure of Apitegromab Biosimilar

Apitegromab Biosimilar is a fully humanized monoclonal antibody that is produced using recombinant DNA technology. 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 specific target, GDF-8, while the constant regions provide stability and effector functions.

The structure of Apitegromab Biosimilar is similar to that of the endogenous human antibodies, which reduces the risk of immunogenicity and increases its efficacy. The antibody has a molecular weight of approximately 150 kDa and a half-life of 21 days, making it suitable for therapeutic use.

Mechanism of Action of Apitegromab Biosimilar

Apitegromab Biosimilar works by binding to GDF-8 and preventing its interaction with its receptor, activin type II receptor (ActRII). This binding inhibits the downstream signaling pathways, such as Smad2/3, which are responsible for regulating muscle growth and differentiation. By blocking the activity of GDF-8, Apitegromab Biosimilar promotes muscle growth and regeneration.

Moreover, Apitegromab Biosimilar also has an Fc region that can interact with immune cells, such as natural killer (NK) cells and macrophages, leading to the destruction of GDF-8-expressing cells. This effector function of the antibody further enhances its therapeutic potential.

Applications of Apitegromab Biosimilar

Apitegromab Biosimilar has potential applications in the treatment of various muscle-wasting disorders, including Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and sarcopenia. These conditions are characterized by a loss of muscle mass and strength, and GDF-8 has been identified as a key factor in their pathogenesis.

Preclinical studies have shown promising results for Apitegromab Biosimilar in animal models of DMD and BMD. It has been found to increase muscle mass and strength, improve muscle function, and reduce fibrosis. The antibody has also been shown to have a synergistic effect when used in combination with other therapies, such as corticosteroids, in DMD treatment.

Furthermore, Apitegromab Biosimilar has potential applications in sports medicine, where it can be used to enhance muscle growth and improve performance. It can also be used in the treatment of age-related muscle loss, or sarcopenia, which is a common problem in the elderly population.

Conclusion

In summary, Apitegromab Biosimilar is a research grade therapeutic antibody that targets GDF-8 and promotes muscle growth and regeneration. Its humanized structure, specific mechanism of action, and potential applications make it a promising candidate for the treatment of muscle-wasting disorders. Further research and clinical trials are needed to fully explore the therapeutic potential of this antibody.

Publication

Sakellariou, P., Walpurgis, K., Thomas, A. et al. Combined detection of inhibitors of the activin receptor signaling pathways (IASPs) by means of LC-HRMS/MS for human doping control. Sci Rep 15, 19887 (2025). https://doi.org/10.1038/s41598-025-03562-y

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