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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Ladiratuzumab Biosimilar - Anti-SLC39A6 mAb - Research Grade |
|---|---|
| Source | CAS 1629760-28-6 |
| Species | Humanized |
| 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 |
| Aliases /Synonyms | Ladiratuzumab,hLIV22,SLC39A6,anti-SLC39A6 |
| Reference | PX-TA1484 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Ladiratuzumab Biosimilar – Anti-SLC39A6 mAb – Research Grade: A Promising Antibody for Targeting SLC39A6 in
Ladiratuzumab Biosimilar (LB) is a monoclonal antibody (mAb) that targets the SLC39A6 protein, also known as ZIP6, which plays a crucial role in the regulation of zinc transport and homeostasis. This antibody has shown promising results in preclinical studies and is currently being developed as a potential therapeutic agent for various types of cancer. In this article, we will discuss the structure, activity, and potential applications of LB as a research-grade antibody.
LB is a fully humanized IgG1 monoclonal antibody with a molecular weight of approximately 150 kDa. It is composed of two heavy chains and two light chains, each containing a variable and constant region. The variable region of the antibody is responsible for binding to the target protein, SLC39A6, while the constant region mediates effector functions such as antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC).
LB specifically binds to the extracellular domain of SLC39A6, which is overexpressed in various types of cancer cells, including breast, lung, and pancreatic cancer. This binding leads to the inhibition of zinc uptake and disrupts zinc homeostasis in cancer cells, ultimately resulting in cell death. LB has also been shown to induce ADCC and CDC, further enhancing its anti-tumor activity.
cancer effects, LB has also been found to sensitize cancer cells to chemotherapy and radiation therapy. This is due to the fact that SLC39A6 plays a critical role in the repair of DNA damage, and inhibition of this protein by LB can increase the efficacy of these treatments.
LB is currently being investigated as a potential therapeutic agent for various types of cancer, including triple-negative breast cancer, non-small cell lung cancer, and pancreatic cancer. Preclinical studies have shown that LB has potent anti-tumor activity, both as a monotherapy and in combination with other treatments.
LB is also being developed as a research-grade antibody for use in laboratory studies. Its specificity for SLC39A6 makes it a valuable tool for studying the role of this protein in cancer biology and for identifying potential biomarkers for patient selection and response to treatment.
LB has also shown potential as a diagnostic tool for detecting SLC39A6 expression in cancer cells. This could aid in the diagnosis and prognosis of certain types of cancer and help guide treatment decisions.
Ladiratuzumab Biosimilar is a promising antibody that specifically targets the SLC39A6 protein, which is overexpressed in various types of cancer. Its unique mechanism of action, including the disruption of zinc homeostasis and induction of ADCC and CDC, makes it a potential therapeutic agent for cancer treatment. In addition, LB has applications as a research-grade antibody and a potential diagnostic tool. Further clinical studies are needed to fully evaluate the efficacy and safety of LB, but early results are promising, and it has the potential to make a significant impact in the field of cancer treatment.
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