Taiy Chemical
TGF α (1-50) (rat)
Synonym TGF alpha (1-50) (rat)
Species Rat
Protein Accession P01135
Purity Greater than 95% by SDS-PAGE
Endotoxin Level < 0.1 ng per μg of protein
Biological Activity The ED50 was determined by a cytotoxicity assay using murine Balb/c 3T3 cells is ≤ 1 ng/ml, corresponding to a specific activity of ≥ 1 x 10^6 units/mg.
Expression System E. coli
Fusion Tag No
Predicted Molecular Mass Approximately 5 kDa
Formulation Lyophilized from a 0.2 μm filtered solution of 20 mM acetic acid
Reconstitution It is recommended to reconstitute the lyophilized product with sterile water at a concentration of 0.1 mg/ml, which can be further diluted into other aqueous solutions
Storage & Stability Store lyophilized protein at -20°C to -80°C. Upon reconstitution, store at 4°C for up to two weeks or aliquot and store at -20°C to -80°C for longer periods. Avoid repeated freeze-thaw cycles.
FAQ
What is TGF α (1-50) (rat) and how does it influence scientific research on cell growth?

Transforming Growth Factor alpha (TGF α) is a polypeptide growth factor that is closely related to the epidermal growth factor (EGF) family. The sequence TGF α (1-50) refers to a segment of this growth factor that includes the amino acids 1 through 50. This particular segment of TGF α has been of considerable interest in scientific research due to its significant influence on cellular growth and development. In the realm of research, TGF α (1-50) from rats serves as a crucial model for studying this growth factor’s role and mechanisms in various biological contexts, especially those related to cell proliferation and differentiation. Researchers are particularly interested in TGF α due to its ability to bind to the EGF receptor (EGFR), initiating a cascade of cellular processes that promote growth, survival, and repair of tissues. The rat model is commonly used because rats share substantial physiological similarities with humans, making them an ideal choice for preclinical studies.

Understanding the mechanisms of TGF α (1-50) is pivotal for developing therapeutic interventions in conditions characterized by abnormal cell growth, such as cancer or regenerative tissue repair. Researchers analyze how this protein segment interacts with cellular receptors and stimulates signal pathways to influence cell cycle regulation. Techniques such as molecular cloning, protein purification, and structural biology have enabled scientists to delve deep into the structural and functional nuances of TGF α. The insights garnered from these studies contribute to the broader field of growth factor research and hold potential for translational research where findings are used to develop new therapeutic strategies. In summary, TGF α (1-50) (rat) is a central component in advancing our understanding of growth factor biology, providing critical insights necessary for therapeutic advances in medicine.

How is TGF α (1-50) (rat) utilized in the study of cancer and tumor biology?

TGF α (1-50) (rat) is extensively utilized in the study of cancer and tumor biology due to its involvement in cell proliferation, differentiation, and survival - processes that are often dysregulated in cancerous tissues. In cancer research, understanding how growth factors like TGF α contribute to tumor development and progression is fundamental. One of the pivotal roles of TGF α is its interaction with the epidermal growth factor receptor (EGFR), which is frequently overexpressed or mutated in various cancers, including breast, lung, and colorectal cancers. This interaction triggers intracellular signaling pathways such as the MAPK, AKT, and STAT pathways, resulting in enhanced cell proliferation and survival, which are hallmarks of cancer.

Researchers studying TGF α (1-50) often use it to investigate how these signaling pathways contribute to oncogenesis and to discern potential therapeutic targets that could disrupt these malignant processes. In vitro studies involving cell lines treated with TGF α (1-50) help delineate the direct effects of this growth factor on cancer cell growth and apoptosis, while in vivo studies in rat models allow researchers to observe the overall impact on tumor progression and metastasis. Furthermore, emerging research leveraging TGF α in personalized medicine approaches aims to tailor anti-cancer therapies based on the specific growth factor and receptor interactions within an individual’s tumor microenvironment.

By understanding how TGF α (1-50) modulates these cellular activities, scientists can design interventions that target these pathways. The ongoing research not only sheds light on the molecular mechanisms underpinning cancer progression but also enhances the development of targeted therapies, such as small molecule inhibitors or monoclonal antibodies against EGFR or its downstream effectors. Thus, the utilization of TGF α (1-50) (rat) in cancer and tumor biology represents a crucial step in translating basic research into effective clinical treatments that improve patient outcomes.

What potential does TGF α (1-50) (rat) have in regenerative medicine and tissue engineering?

TGF α (1-50) (rat) holds significant potential in regenerative medicine and tissue engineering due to its capacity to stimulate cell proliferation and differentiation, which are essential components of tissue repair and regeneration. In regenerative medicine, the primary goal is to restore the function of damaged tissues or organs by promoting the growth of new, healthy cells. TGF α, through its action on the EGFR, plays a pivotal role in these processes by activating signaling pathways that are crucial for cellular growth, survival, and regeneration. The ability of TGF α (1-50) to modulate these pathways provides a unique advantage in directing cellular behavior in a controlled manner, which is essential for effective tissue engineering.

In tissue engineering, scaffolds embedded with growth factors such as TGF α are used to create a supportive environment that facilitates the growth and differentiation of stem cells or progenitor cells into specific tissue types. This growth factor can enhance the regenerative capacity of these cells by promoting their proliferation and facilitating their differentiation into the desired cell lineages. As a result, TGF α (1-50) can be employed in the creation of bioengineered tissues that can potentially replace damaged tissues in vivo, improving healing outcomes and functional restoration.

Research in this field focuses on optimizing the delivery methods of TGF α (1-50) to ensure sustained and localized release at the site of tissue repair. Biomaterials that can incorporate TGF α and release it in a controlled fashion are being developed to increase the efficacy of these regenerative treatments. Moreover, the integration of TGF α into 3D-printed scaffolds or hydrogel-based systems represents a cutting-edge approach to fabricating complex tissue structures with the potential to revolutionize regenerative therapies. By leveraging the regenerative properties of TGF α (1-50), scientists aim to advance tissue engineering strategies that could lead to breakthroughs in repairing tissues such as skin, bone, cartilage, and even organs, paving the way for new treatments in regenerative medicine.

How does TGF α (1-50) (rat) impact studies related to wound healing and dermatological research?

TGF α (1-50) (rat) plays a significant role in studies related to wound healing and dermatological research due to its ability to promote cell proliferation, migration, and differentiation—processes that are pivotal in the repair and regeneration of skin tissue. In the context of wound healing, TGF α acts as a potent mitogen for epithelial cells, which are essential for the re-epithelialization phase of wound repair. This growth factor's interaction with the EGFR on keratinocytes and other skin cells initiates signaling pathways that stimulate these cells to divide and migrate to the wound site, facilitating the closure of wounds.

Researchers are particularly interested in TGF α (1-50) for its application in enhancing wound healing outcomes. Studies involving this growth factor aim to delineate the molecular mechanisms by which it accelerates the healing process and improves the strength and integrity of repaired tissue. This is achieved by investigating its effects on various cellular and molecular components of the skin, including fibroblasts, collagen production, and extracellular matrix remodeling. In vitro and in vivo models, including rat wound healing models, are extensively used to assess the efficacy of TGF α in promoting faster and more efficient healing of skin injuries.

Furthermore, in dermatological research, TGF α (1-50) is explored for its potential in treating skin disorders characterized by impaired wound healing or chronic ulcerations, such as diabetic ulcers or pressure sores. By enhancing keratinocyte proliferation and migration, TGF α may help overcome the healing deficiencies observed in such conditions. Moreover, the cosmetic industry is exploring the potential benefits of TGF α in anti-aging treatments due to its capacity to stimulate the renewal of skin cells and its role in maintaining skin elasticity and firmness.

Overall, the impact of TGF α (1-50) (rat) on wound healing and dermatological research is profound, providing valuable insights into the complex biology of wound repair and offering promising avenues for developing new therapeutic applications to enhance skin regeneration and address various dermatological conditions.

What role does TGF α (1-50) (rat) play in the study of neurological disorders or brain injuries?

TGF α (1-50) (rat) plays a noteworthy role in the study of neurological disorders and brain injuries due to its involvement in neural development, repair processes, and neuroprotection. In the central nervous system, growth factors like TGF α are crucial for the proliferation and differentiation of neural progenitor cells, thereby influencing neurogenesis and the maintenance of neural tissues. Researchers investigating neurodegenerative diseases, such as Alzheimer’s and Parkinson’s disease, or acute brain injuries, such as trauma or stroke, are particularly interested in understanding how TGF α can modulate neural repair and recovery processes.

The significance of TGF α (1-50) in neurological research primarily centers around its ability to interact with neural receptors and activate signaling pathways that promote cell survival and reduce apoptosis in neurons. This growth factor is being studied for its potential neuroprotective effects, which include the ability to mitigate oxidative stress and inflammation commonly associated with neurodegenerative processes. In animal models, including those involving rats, TGF α has been shown to enhance the survival of neurons and support the regeneration of neural tissues following injury, suggesting its therapeutic potential in mitigating the effects of neurological disorders.

Moreover, TGF α is explored for its role in glial cell function, particularly in astrocyte and oligodendrocyte biology, which are vital for maintaining neural health and facilitating repair after injury. Researchers utilize TGF α (1-50) to study how it affects the glial response to CNS injuries and its ability to ameliorate demyelination or neuronal loss. The potential of TGF α to facilitate remyelination and neuroprotection presents a promising avenue for developing strategies to treat conditions characterized by neural damage, such as multiple sclerosis.

In summary, TGF α (1-50) (rat) plays a critical role in advancing our understanding of the biological processes involved in neuroprotection and neural repair, offering potential insights for developing novel therapeutic interventions for neurological disorders and brain injuries. By leveraging the regenerative and protective properties of TGF α, researchers aim to improve outcomes for individuals affected by these debilitating conditions.
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