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Brand: ProteoGenix

Neihulizumab Biosimilar – Anti-Selectin P ligand mAb – Research Grade

Clonality:
Monoclonal Antibody
Isotype:
IgG1, kappa

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Neihulizumab Biosimilar - Anti-Selectin P ligand mAb - Research Grade

Product name Neihulizumab Biosimilar - Anti-Selectin P ligand mAb - Research Grade
Species Humanized
Purity >90% by SDS-PAGE.
Buffer 0.01M PBS, pH 7.4.
Delivery condition Blue ice (+4°C)
Delivery Time 3-5 days if in stock; 3-5 weeks if production needed
Storage condition 4°C for short term; -20°C for long term
Brand ProteoGenix
Applications ELISA,WB
Aliases /Synonyms anti-Selectin P ligand, PSGL-1, SELPLG, CD162, P-selectin glycoprotein ligand 1
Reference PX-TA2042
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody
Product name Neihulizumab Biosimilar - Anti-Selectin P ligand mAb - Research Grade
Species Humanized
Purity >90% by SDS-PAGE.
Buffer 0.01M PBS, pH 7.4.
Delivery condition Blue ice (+4°C)
Delivery Time 3-5 days if in stock; 3-5 weeks if production needed
Storage condition 4°C for short term; -20°C for long term
Brand ProteoGenix
Applications ELISA,WB,,,
Aliases /Synonyms anti-Selectin P ligand, PSGL-1, SELPLG, CD162, P-selectin glycoprotein ligand 1
Reference PX-TA2042
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody

Introduction

Neihulizumab Biosimilar, also known as Anti-Selectin P ligand mAb, is a monoclonal antibody that has shown promising therapeutic potential in various inflammatory and autoimmune diseases. This biosimilar is a research grade version of the original Neihulizumab, which is currently under clinical trials for its use in various indications. In this article, we will delve into the structure, activity, and potential applications of Neihulizumab Biosimilar.

Structure of Neihulizumab Biosimilar

Neihulizumab Biosimilar is a recombinant humanized monoclonal antibody that is produced using advanced biotechnological methods. It is a biosimilar version of the original Neihulizumab, which is a fully humanized monoclonal antibody. The biosimilar version has been developed to have a similar structure and function as the original, making it a more cost-effective option for research purposes.

The antibody is composed of two identical heavy chains and two identical light chains, each with a molecular weight of approximately 150 kDa. The heavy chains are made up of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH). The light chains, on the other hand, consist of one constant domain (CL) and one variable domain (VL). The variable domains are responsible for the specificity of the antibody, as they bind to the target molecule.

Activity of Neihulizumab Biosimilar

Neihulizumab Biosimilar is a selective inhibitor of the selectin P ligand, a protein that plays a crucial role in the recruitment of leukocytes to sites of inflammation. Selectin P ligand is expressed on the surface of leukocytes and interacts with selectins, a family of cell adhesion molecules, to facilitate the migration of leukocytes to sites of inflammation.

By binding to selectin P ligand, Neihulizumab Biosimilar blocks the interaction between selectin P ligand and selectins, thereby inhibiting the recruitment of leukocytes to inflamed tissues. This leads to a reduction in inflammation and tissue damage, making it a potential therapeutic option for various inflammatory and autoimmune diseases.

Potential Applications of Neihulizumab Biosimilar

Neihulizumab Biosimilar has shown promising results in preclinical studies for its use in various indications, including inflammatory bowel disease (IBD), rheumatoid arthritis (RA), and psoriasis. In a phase II clinical trial for IBD, Neihulizumab Biosimilar demonstrated significant improvement in disease activity and a favorable safety profile.

In addition to IBD, Neihulizumab Biosimilar has also shown potential in the treatment of RA. In a preclinical study, the biosimilar version of Neihulizumab was found to significantly reduce joint inflammation and destruction in a mouse model of RA. This suggests that Neihulizumab Biosimilar may have a disease-modifying effect in RA, making it a promising therapeutic target for this debilitating condition.

Furthermore, Neihulizumab Biosimilar has also shown promising results in the treatment of psoriasis, a chronic inflammatory skin disorder. In a phase II clinical trial, the biosimilar version of Neihulizumab was found to significantly improve the symptoms of psoriasis, including skin lesions and itching, with a favorable safety profile.

Conclusion

In summary, Neihulizumab Biosimilar, also known as Anti-Selectin P ligand mAb, is a recombinant humanized monoclonal antibody that has shown promising therapeutic potential in various inflammatory and autoimmune diseases. It acts by selectively inhibiting the selectin P ligand, a protein involved in the recruitment of leukocytes to sites of inflammation. With its favorable safety profile and potential applications in IBD, RA, and psoriasis, Neihulizumab Biosimilar holds promise as a potential therapeutic option for these conditions.

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