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.