Gene: GALT
Official Full Name: galactose-1-phosphate uridylyltransferaseprovided by HGNC
Gene Summary: Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00262 | GALT Knockout cell line (HEK293) | Human | GALT | 1:3~1:6 | Negative | Online Inquiry |
GALT Gene Knockout Cell Lines are specialized cellular models engineered to lack the gene encoding galactose-1-phosphate uridylyltransferase (GALT), an enzyme critical for galactose metabolism. These cell lines are invaluable tools for studying galactosemia, a metabolic disorder characterized by an inability to metabolize galactose properly, leading to serious health implications if left untreated. By utilizing these knockout lines, researchers can explore the fundamental biological processes disrupted in GALT deficiency, allowing for a deeper understanding of metabolic pathways and the development of potential therapies.
The primary function of GALT Gene Knockout Cell Lines lies in their ability to simulate the pathophysiological conditions of galactosemia. Lacking functional GALT, these cell lines accumulate toxic levels of galactose and its metabolites, which researchers can monitor to elucidate their specific roles in cellular dysfunction. The cell lines facilitate various experimental approaches, including drug screening, gene therapy studies, and the evaluation of dietary interventions, providing a robust platform for therapeutic development.
Scientifically, GALT knockout models hold significant importance in both research and clinical contexts. They offer a means of validating potential treatments and understanding the cellular response to galactose, which is crucial for developing strategies to mitigate the effects of this metabolic disorder. Additionally, these models can significantly enhance preclinical studies and inform clinical practice by bridging knowledge gaps in this field.
What sets our GALT Gene Knockout Cell Lines apart from conventional cell models is their precision-engineered deficiency, which ensures reproducibility and reliability for rigorous scientific inquiry. Unlike alternatives that may possess residual GALT activity, our cell lines provide a truly consistent environment to study GALT-related disorders, making them essential for high-quality research.
For researchers and clinicians focused on metabolic diseases, the value of these cell lines lies in their ability to accelerate the translation of bench research into clinical applications. They open avenues for innovation in understanding and treating galactosemia, promoting improved patient outcomes.
Our company prides itself on its deep expertise in cell line development and spanning a range of conditions. We are committed to providing high-quality biological products that empower researchers to make groundbreaking advancements in medical science.
Please note that all services are for research use only. Not intended for any clinical use.
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