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Brand: ProteoGenix

Tisotumab Biosimilar – Anti-F3 , CD142 mAb – Research Grade

  • PX-TA1402
Clonality:
Monoclonal Antibody
Isotype:
IgG1, kappa

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Tisotumab Biosimilar - Anti-F3 , CD142 mAb - Research Grade

Product name Tisotumab Biosimilar - Anti-F3 , CD142 mAb - Research Grade
Source CAS 1418628-81-5
Species Homo sapiens
Purity >85%
Buffer PBS buffer PH7.5
Delivery condition Blue ice (+4°C)
Delivery Time 3-5 days if in stock; 3-5 weeks if production needed
Storage condition store at -80°C
Brand ProteoGenix
Applications ELISA,WB
Aliases /Synonyms Tisotumab,HuMax-TF,F3 , CD142,anti-F3 , CD142
Reference PX-TA1402
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody
Product name Tisotumab Biosimilar - Anti-F3 , CD142 mAb - Research Grade
Source CAS 1418628-81-5
Species Homo sapiens
Purity >85%
Buffer PBS buffer PH7.5
Delivery condition Blue ice (+4°C)
Delivery Time 3-5 days if in stock; 3-5 weeks if production needed
Storage condition store at -80°C
Brand ProteoGenix
Applications ELISA,WB,,,
Aliases /Synonyms Tisotumab,HuMax-TF,F3 , CD142,anti-F3 , CD142
Reference PX-TA1402
Note For research use only. Not suitable for clinical or therapeutic use.
Isotype IgG1-kappa
Clonality Monoclonal Antibody

Introduction

Tisotumab Biosimilar – Anti-F3, CD142 mAb – Research Grade is a novel antibody that has shown promising results in the treatment of various types of cancer. This biosimilar is designed to target the F3 protein, also known as CD142, which is overexpressed in many cancer types and has been identified as a potential therapeutic target.

Structure of Tisotumab Biosimilar

Tisotumab Biosimilar is a monoclonal antibody (mAb) that is produced through recombinant DNA technology. It is a fully human antibody, meaning that it is derived from human cells and has a structure identical to natural human antibodies. This makes it less likely to cause an immune response in patients, making it a safer and more effective treatment option.

The antibody is composed of two heavy chains and two light chains, each containing specific regions that are responsible for its binding and therapeutic activity. The heavy chains are connected to each other by disulfide bonds, while the light chains are connected to the heavy chains by non-covalent interactions.

Activity of Tisotumab Biosimilar

Tisotumab Biosimilar specifically targets the F3 protein, which is a member of the tissue factor (TF) family. F3 is a transmembrane glycoprotein that plays a crucial role in the initiation of blood coagulation. It is also involved in various cellular processes such as angiogenesis, cell migration, and proliferation.

In cancer cells, F3 is overexpressed and promotes tumor growth, metastasis, and resistance to chemotherapy. Tisotumab Biosimilar binds to F3 and blocks its activity, inhibiting the growth and spread of cancer cells. It also triggers an immune response against cancer cells, leading to their destruction.

Application of Tisotumab Biosimilar

Tisotumab Biosimilar has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of various types of cancer, including cervical, ovarian, and lung cancer. It has also shown potential in combination with other cancer therapies, such as chemotherapy and radiation therapy.

In addition to its therapeutic application, Tisotumab Biosimilar also has potential diagnostic and prognostic uses. F3 is overexpressed in many cancer types, and its levels can be measured in blood samples. This can help in the early detection and monitoring of cancer progression.

Conclusion

Tisotumab Biosimilar – Anti-F3, CD142 mAb – Research Grade is a novel antibody that has shown promising results in the treatment of various types of cancer. Its unique structure, targeting the F3 protein, and triggering an immune response make it a potential therapeutic option for cancer patients. Further research and clinical trials are needed to fully understand its efficacy and potential applications in cancer treatment.

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