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Urtoxazumab Biosimilar – Anti-Stx-2, SLT-II 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 nameUrtoxazumab Biosimilar - Anti-Stx-2, SLT-II mAb - Research Grade
SourceCAS 502496-16-4
SpeciesHumanized
Expression systemMammalian cells
Purity>85%
BufferPBS buffer PH7.5
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3-5 weeks if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsUrtoxazumab,HuVTm1.1,TMA-15,Stx-2, SLT-II,anti-Stx-2, SLT-II
ReferencePX-TA1190
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1-kappa
ClonalityMonoclonal Antibody

Description of Urtoxazumab Biosimilar - Anti-Stx-2, SLT-II mAb - Research Grade

Introduction

Urtoxazumab Biosimilar – Anti-Stx-2, SLT-II mAb – Research Grade is a monoclonal antibody that has been developed as a biosimilar to Urtoxazumab, a therapeutic antibody used in the treatment of Shiga toxin-producing E. coli (STEC) infections. This biosimilar has been designed to specifically target Stx-2, one of the main toxins produced by STEC, making it a promising therapeutic option for patients with STEC infections.

Structure of Urtoxazumab Biosimilar

Urtoxazumab Biosimilar is a monoclonal antibody, meaning it is produced by a single type of immune cell and is therefore highly specific in its target binding. The antibody is composed of two identical heavy chains and two identical light chains, connected by disulfide bonds. The heavy chains contain a variable region, responsible for binding to the target, and a constant region, which determines the antibody’s class and effector functions. The light chains also have a variable and constant region, but are smaller in size compared to the heavy chains.

Activity of Urtoxazumab Biosimilar

The main activity of Urtoxazumab Biosimilar is to bind to Stx-2, preventing it from binding to its target receptors on host cells. Stx-2 is a potent toxin produced by STEC, which can cause severe gastrointestinal and neurological symptoms in infected individuals. By binding to Stx-2, Urtoxazumab Biosimilar prevents the toxin from entering host cells and causing damage. This neutralizing activity of the biosimilar can help in reducing the severity of symptoms and improving the outcome of STEC infections.

In addition to its neutralizing activity, Urtoxazumab Biosimilar also has effector functions that can help in clearing Stx-2 from the body. These include antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). In ADCC, the antibody binds to Stx-2 and recruits immune cells, such as natural killer cells, to destroy the target. In CDC, the antibody binds to Stx-2 and activates the complement system, leading to the lysis of the target.

Application of Urtoxazumab Biosimilar

Urtoxazumab Biosimilar has shown promising results in preclinical studies as a potential treatment for STEC infections. Its specificity and neutralizing activity make it a promising alternative to Urtoxazumab, which has shown limited efficacy in clinical trials. The biosimilar can also be used as a prophylactic treatment for individuals at high risk of STEC infections, such as those with compromised immune systems.

In addition to its therapeutic potential, Urtoxazumab Biosimilar can also be a valuable tool in research and diagnostics. Its specificity for Stx-2 makes it a useful reagent for detecting and quantifying the toxin in clinical samples. It can also be used in research studies to better understand the mechanisms of STEC infections and develop new treatments.

Conclusion

In summary, Urtoxazumab Biosimilar – Anti-Stx-2, SLT-II mAb – Research Grade is a monoclonal antibody that specifically targets Stx-2, a toxin produced by STEC. Its structure, activity, and applications make it a promising therapeutic option for STEC infections, as well as a valuable tool in research and diagnostics. Further clinical trials are needed to evaluate the efficacy and safety of this biosimilar, but it holds great potential in improving the treatment and prevention of STEC infections.

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