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| Size | 100ug, 1MG |
|---|---|
| Brand | ProteoGenix |
| Product type | Recombinant Proteins |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Balugrastim Biosimilar - Anti-G-CSF receptor fusion protein - Research Grade |
|---|---|
| Species | Homo sapiens |
| Expression system | XtenCHO |
| Purity | >90% by SDS-PAGE. |
| Buffer | 0.01M PBS, pH 7.4. |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | 4°C for short term; -20°C for long term |
| Brand | ProteoGenix |
| Aliases /Synonyms | anti-G-CSF receptor, CSF3R, GCSFR, G-CSF-R, CD114, Granulocyte colony-stimulating factor receptor |
| Reference | PX-TA2033 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | Fusion - [ALB (albumin, human serum albumin, HSA) 25-609 - CSF3 (colony stimulating factor 3, GCSF, granulocyte colony-stimulating factor, G-CSF)] |
Introduction to Balugrastim Biosimilar – A Promising Anti-G-CSF Receptor Fusion Protein Balugrastim Biosimilar is a novel biologic agent designed to mimic the activity of the naturally occurring human granulocyte colony-stimulating factor (G-CSF). It is a fusion protein that targets the G-CSF receptor, making it a potential therapeutic option for a variety of conditions related to impaired immune function. In this article, we will delve into the structure, activity, and potential applications of Balugrastim Biosimilar.
Balugrastim Biosimilar is a recombinant fusion protein consisting of two distinct parts – a human G-CSF receptor binding domain and a human IgG1 Fc domain. The G-CSF receptor binding domain is responsible for the specific targeting of the G-CSF receptor, while the Fc domain provides stability and prolongs the half-life of the drug. The structure of Balugrastim Biosimilar is similar to that of endogenous G-CSF, allowing it to bind and activate the G-CSF receptor with high specificity and potency.
The primary function of Balugrastim Biosimilar is to stimulate the production and maturation of neutrophils, a type of white blood cell involved in immune defense. This is achieved by binding to and activating the G-CSF receptor, which is expressed on the surface of hematopoietic stem cells and mature neutrophils. Activation of the G-CSF receptor leads to the proliferation and differentiation of these cells, resulting in an increase in the number of mature neutrophils in the blood.
Due to its ability to stimulate the production of neutrophils, Balugrastim Biosimilar has potential applications in a variety of conditions related to impaired immune function. These include:
1. Neutropenia: Neutropenia is a condition characterized by a low number of neutrophils in the blood, which can increase the risk of infections. Balugrastim Biosimilar can be used to treat neutropenia in patients undergoing chemotherapy or bone marrow transplantation.
2. Inflammatory Bowel Disease (IBD): IBD is a chronic inflammatory condition of the gastrointestinal tract. Balugrastim Biosimilar has shown promise in clinical trials as a potential treatment for IBD, as it can promote the migration of neutrophils to the site of inflammation, thereby reducing inflammation.
3. Wound Healing: Neutrophils play a crucial role in wound healing by clearing bacteria and debris from the site of injury. Balugrastim Biosimilar can potentially accelerate wound healing by promoting the recruitment and activation of neutrophils.
4. Sepsis: Sepsis is a life-threatening condition caused by a dysregulated immune response to an infection. Balugrastim Biosimilar has been shown to improve survival rates in animal models of sepsis by increasing the number of neutrophils and enhancing their antibacterial activity.
In conclusion, Balugrastim Biosimilar is a promising anti-G-CSF receptor fusion protein with potential applications in various conditions related to impaired immune function. Its unique structure and activity make it a promising therapeutic option for patients in need of immune support. Further research and clinical trials are needed to fully understand the potential of this novel biologic agent.
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