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Brand: ProteoGenix

Anti-Human Non-native TTR/Prealbumin/TransthyretinR Monoclonal Antibody, SAA0813

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Anti-Human Non-native TTR/Prealbumin/TransthyretinR Monoclonal Antibody, SAA0813

Product name Anti-Human Non-native TTR/Prealbumin/TransthyretinR Monoclonal Antibody, SAA0813
Form 0.01M PBS, pH 7.4.
Delivery condition Blue ice (+4°C)
Storage condition 4°C for short term (1 week), store at -20°C to -80°C for long term(1 year); Avoid repeated freeze-thaw cycles
Brand ProteoGenix
Host species Mouse
Reactivity Human
Reference PTX19328
Isotype IgG1, kappa
Clonality Monoclonal Antibody
Purification Protein A or G purified from cell culture supernatant.
Immunogen Transthyretin, Prealbumin, TBPA, TTR, PALB, ATTR, non-native TTR
Clone Name SAA0813
Format Liquid
Background information Array
Target species Anti-Human Monoclonal Antibody

Introduction

Anti-Human Non-native TTR/Prealbumin/TransthyretinR Monoclonal Antibody, also known as SAA0813, is a therapeutic antibody that targets transthyretin (TTR) and prealbumin (PA) proteins. This antibody has been extensively studied for its potential use in treating various diseases, making it a promising candidate for further research and development.

Structure

SAA0813 is a monoclonal antibody, meaning it is derived from a single clone of immune cells. It is designed to specifically target and bind to the non-native form of transthyretin, which is a protein that plays a crucial role in transporting thyroid hormones and retinol in the body. The antibody has a unique structure that allows it to bind to non-native TTR and PA proteins with high affinity and specificity.

Activity

The main activity of SAA0813 is to inhibit the aggregation of non-native TTR and PA proteins. These proteins have been linked to various diseases, including familial amyloidotic polyneuropathy (FAP) and senile systemic amyloidosis (SSA). In these diseases, the misfolding and aggregation of TTR and PA proteins can lead to the formation of amyloid deposits, which can cause tissue damage and organ dysfunction. By binding to non-native TTR and PA proteins, SAA0813 prevents their aggregation, thereby reducing the formation of amyloid deposits.

Therapeutic Target

SAA0813 is a promising therapeutic target for the treatment of diseases associated with non-native TTR and PA proteins. FAP and SSA are the two main diseases that have been targeted by this antibody. FAP is a rare genetic disorder characterized by the accumulation of amyloid deposits in peripheral nerves, leading to progressive nerve damage and loss of function. SSA, on the other hand, is a non-inherited disease that primarily affects the heart and other organs. By inhibiting the aggregation of non-native TTR and PA proteins, SAA0813 has the potential to slow down or even reverse the progression of these diseases.

Research Use

Apart from its potential as a therapeutic agent, SAA0813 is also widely used in research studies. Its ability to specifically target and bind to non-native TTR and PA proteins makes it a valuable tool for studying the role of these proteins in various diseases. Researchers can use this antibody to investigate the mechanisms underlying the misfolding and aggregation of TTR and PA proteins, as well as to develop new diagnostic and therapeutic strategies.

Application

SAA0813 has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of FAP and SSA. The antibody is administered through intravenous infusion, and early results have shown that it is well-tolerated and has the potential to improve disease outcomes. In addition, SAA0813 has also been investigated for its potential use in treating other diseases, such as Alzheimer’s and Parkinson’s, which are also associated with the aggregation of amyloid proteins.

Conclusion

In conclusion, Anti-Human Non-native TTR/Prealbumin/TransthyretinR Monoclonal Antibody, SAA0813, is a promising therapeutic agent with the potential to treat diseases associated with non-native TTR and PA proteins. Its unique structure and activity make it a valuable tool for research studies, and its application in clinical trials holds promise for improving the lives of patients with FAP and SSA. Further research and development of this antibody may lead to new treatment options for other diseases as well.

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