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Tacatuzumab Biosimilar – Anti-Alpha-fetoprotein mAb – Research Grade

Reference:
Size

100µg, 1MG

Isotype

IgG1, kappa

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa, WB

Product nameTacatuzumab Biosimilar - Anti-Alpha-fetoprotein mAb - Research Grade
SpeciesHumanized
Expression systemXtenCHO
BufferPBS buffer PH7.5
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-Alpha-fetoprotein,Alpha-1-fetoprotein,Alpha-fetoglobulin,AFP,HPAFP,
ReferencePX-TA1906
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1-kappa
ClonalityMonoclonal Antibody

Description of Tacatuzumab Biosimilar - Anti-Alpha-fetoprotein mAb - Research Grade

The Structure of Tacatuzumab Biosimilar – Anti-Alpha-fetoprotein mAb

Tacatuzumab Biosimilar, also known as Anti-Alpha-fetoprotein mAb, is a monoclonal antibody that has been designed to target the alpha-fetoprotein (AFP) protein. This protein is highly expressed in certain types of cancer, including liver, ovarian, and testicular cancer, making it a promising therapeutic target.

The structure of Tacatuzumab Biosimilar is based on the original monoclonal antibody, which was developed using recombinant DNA technology. It is a chimeric antibody, meaning that it contains both human and mouse components. This is important for its therapeutic use, as it reduces the risk of an immune response against the antibody in patients.

The antibody is composed of four protein chains, two heavy chains and two light chains, each with a specific function. The heavy chains are responsible for the antibody’s binding to the AFP protein, while the light chains help with stability and function.

The Activity of Tacatuzumab Biosimilar

The main activity of Tacatuzumab Biosimilar is its ability to bind to the AFP protein with high specificity and affinity. This means that it can recognize and attach to the AFP protein, which is overexpressed in cancer cells, while leaving healthy cells unharmed.

Once bound to the AFP protein, Tacatuzumab Biosimilar can activate the body’s immune system to attack and destroy cancer cells. This is known as antibody-dependent cell-mediated cytotoxicity (ADCC), and it is one of the main mechanisms of action for monoclonal antibodies.

In addition to its direct anti-

cancer activity, Tacatuzumab Biosimilar has also been shown to have anti-angiogenic properties. This means that it can inhibit the growth of new blood vessels that supply nutrients to cancer cells, further limiting their growth and spread.

Applications of Tacatuzumab Biosimilar

Tacatuzumab Biosimilar is currently being researched for its potential use in the treatment of various types of cancer, including liver, ovarian, and testicular cancer. It is also being studied for its potential as a diagnostic tool, as AFP levels are often used as a biomarker for certain types of cancer.

One of the main advantages of Tacatuzumab Biosimilar is its potential to be used in combination with other cancer treatments, such as chemotherapy and radiation therapy. This is because it has a different mechanism of action and can target cancer cells that may be resistant to other treatments.

In addition to its therapeutic potential, Tacatuzumab Biosimilar is also being studied for its use in research and development of new cancer treatments. Its high specificity and affinity for the AFP protein make it a valuable tool for studying the role of AFP in cancer and developing new therapies that target this protein.

Conclusion

In summary, Tacatuzumab Biosimilar – Anti-Alpha-fetoprotein mAb – Research Grade is a promising monoclonal antibody with a unique structure and multiple mechanisms of action. Its ability to specifically target the AFP protein and activate the immune system make it a potential treatment option for various types of cancer. With ongoing research and development, Tacatuzumab Biosimilar has the potential to improve outcomes for cancer patients and contribute to the advancement of cancer treatment.

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