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Crovalimab Biosimilar – Anti-C5 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 nameCrovalimab Biosimilar - Anti-C5 mAb - Research Grade
SourceCAS 1917321-26-6
SpeciesHumanized
Expression systemMammalian cells
Purity>85%
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; 3-5 weeks if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsCrovalimab,RG-6107,RO7112689,SKY-59,C5,anti-C5
ReferencePX-TA1497
NoteFor research use only. Not suitable for human use.
IsotypeIgG1, kappa
ClonalityMonoclonal Antibody

Description of Crovalimab Biosimilar - Anti-C5 mAb - Research Grade

The Structure of Crovalimab Biosimilar

Crovalimab Biosimilar, also known as Anti-C5 mAb, is a monoclonal antibody that targets the complement protein C5. This biosimilar is a highly specific and potent antibody that is designed to mimic the structure and function of the original drug, eculizumab. Crovalimab Biosimilar is a research grade antibody that is currently being developed for the treatment of various complement-mediated diseases.

Structure of Crovalimab Biosimilar

Crovalimab Biosimilar is a recombinant humanized IgG2/4κ monoclonal antibody. 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 target protein, C5. The constant region of the antibody is responsible for mediating various effector functions, such as complement activation and antibody-dependent cellular cytotoxicity (ADCC).

Mechanism of Action

Crovalimab Biosimilar works by binding to the complement protein C5 and preventing its cleavage into C5a and C5b. This cleavage is a crucial step in the activation of the complement cascade, which is involved in various inflammatory and immune responses. By inhibiting the cleavage of C5, Crovalimab Biosimilar effectively blocks the downstream effects of the complement cascade, leading to a decrease in inflammation and tissue damage.

Therapeutic Applications

Crovalimab Biosimilar is being developed for the treatment of various complement-mediated diseases, including paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), and myasthenia gravis. These diseases are characterized by an overactive complement system, leading to tissue damage and organ dysfunction. By targeting C5, Crovalimab Biosimilar has the potential to provide a targeted and effective treatment for these diseases.

Benefits of Crovalimab Biosimilar

As a research grade antibody, Crovalimab Biosimilar offers several benefits over the original drug, eculizumab. Firstly, it is a more cost-effective option, making it more accessible for patients and healthcare systems. Additionally, being a biosimilar, it has been extensively tested for safety and efficacy, providing reassurance to both patients and healthcare providers. Finally, Crovalimab Biosimilar has the potential to improve patient outcomes by providing a targeted and effective treatment option for complement-mediated diseases.

Conclusion

In summary, Crovalimab Biosimilar is a highly specific and potent monoclonal antibody that targets the complement protein C5. Its unique structure and mechanism of action make it a promising treatment option for various complement-mediated diseases. As a research grade antibody, it offers several benefits over the original drug, making it a more accessible and cost-effective option for patients. With ongoing research and development, Crovalimab Biosimilar has the potential to improve the lives of patients suffering from complement-mediated diseases.

Publication

Profaizer, Tracie and Saadalla, Abdulrahman and Nandakumar, Vijayalakshmi, Validation for Soluble C5b-9 Detection and Comparative Analysis of Three Quantification Methods. Available at SSRN: https://ssrn.com/abstract=4968065 or http://dx.doi.org/10.2139/ssrn.4968065

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