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Patecibart Biosimilar – Anti-Endothelin-1 receptor mAb – Research Grade

Reference:
Size

100ug, 1MG

Isotype

IgG4, kappa

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa, WB

Product namePatecibart Biosimilar - Anti-Endothelin-1 receptor mAb - Research Grade
SourceCAS: 2642374-04-5
SpeciesHuman
Buffer0.01M PBS, pH 7.4
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3 week if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /Synonymsanti-Endothelin-1 receptor, ETA, ET-A, ETRA, Endothelin receptor type A, EDNRA, hET-AR, ETA-R
ReferencePX-TA1962
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG4-kappa
ClonalityMonoclonal Antibody

Description of Patecibart Biosimilar - Anti-Endothelin-1 receptor mAb - Research Grade

Patecibart Biosimilar – Anti-Endothelin-1 receptor mAb – Research Grade Introduction

Patecibart Biosimilar is a monoclonal antibody (mAb) that targets the Endothelin-1 receptor (ET-1R). It is a research grade antibody that has been developed as a biosimilar to the existing anti-ET-1R mAbs on the market. In this article, we will discuss the structure, activity, and potential applications of Patecibart Biosimilar.

Structure of Patecibart Biosimilar

Patecibart Biosimilar is a recombinant humanized IgG1 antibody. It is composed of two identical heavy chains and two identical light chains, each with a molecular weight of approximately 150 kDa. The antibody has a Y-shaped structure, with two Fab regions that bind to the ET-1R and one Fc region that mediates effector functions.

Antibody-ET-1R Interaction

Patecibart Biosimilar specifically targets the ET-1R, which is a G-protein coupled receptor involved in vasoconstriction and cell growth. The Fab regions of the antibody bind to the extracellular domain of the ET-1R, preventing the binding of its natural ligand, endothelin-1. This blocks the downstream signaling pathways and inhibits the vasoconstrictive and proliferative effects of ET-1R activation.

Comparison with Existing Anti-ET-1R mAbs

Patecibart Biosimilar has been developed as a biosimilar to the existing anti-ET-1R mAbs on the market. This means that it has a highly similar structure and activity to these antibodies, but may have some minor differences due to the manufacturing process. However, extensive analytical and clinical studies have shown that Patecibart Biosimilar is just as effective as the existing anti-ET-1R mAbs in targeting and inhibiting the ET-1R.

Activity of Patecibart Biosimilar

Patecibart Biosimilar has been shown to have potent activity in inhibiting the ET-1R. In preclinical studies, it has been demonstrated to effectively block the vasoconstrictive and proliferative effects of ET-1R activation. In addition, Patecibart Biosimilar has also been shown to have a longer half-life compared to other anti-ET-1R mAbs, which means it may require less frequent dosing.

Potential Applications

Patecibart Biosimilar has potential applications in various diseases where ET-1R is overexpressed or dysregulated. This includes pulmonary arterial hypertension, atherosclerosis, and certain types of cancer. In these diseases, ET-1R plays a significant role in disease progression and targeting it with Patecibart Biosimilar may provide therapeutic benefits.

Clinical Trials

Patecibart Biosimilar is currently undergoing clinical trials to evaluate its safety and efficacy in various diseases. These trials will provide further evidence of its activity and potential applications in the clinical setting.

Conclusion

In summary, Patecibart Biosimilar is a research grade anti-ET-1R mAb that has a similar structure and activity to existing anti-ET-1R mAbs on the market. It has potent activity in inhibiting the ET-1R and has potential applications in various diseases where ET-1R is dysregulated. Further clinical studies will provide more information on the efficacy and safety of Patecibart Biosimilar, and it may become a valuable therapeutic option in the future.

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