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GCH1 Knockout Cell Lines

Gene: GCH1

Official Full Name: GTP cyclohydrolase 1provided by HGNC

Gene Summary: This gene encodes a member of the GTP cyclohydrolase family. The encoded protein is the first and rate-limiting enzyme in tetrahydrobiopterin (BH4) biosynthesis, catalyzing the conversion of GTP into 7,8-dihydroneopterin triphosphate. BH4 is an essential cofactor required by aromatic amino acid hydroxylases as well as nitric oxide synthases. Mutations in this gene are associated with malignant hyperphenylalaninemia and dopa-responsive dystonia. Several alternatively spliced transcript variants encoding different isoforms have been described; however, not all variants give rise to a functional enzyme. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO37683 GCH1 Knockout cell line (HeLa) Human GCH1 1:3~1:6 Negative Online Inquiry
KO37684 GCH1 Knockout cell line (HCT 116) Human GCH1 1:2~1:4 Negative Online Inquiry
KO37685 GCH1 Knockout cell line (HEK293) Human GCH1 1:3~1:6 Negative Online Inquiry
KO37686 GCH1 Knockout cell line (A549) Human GCH1 1:3~1:4 Negative Online Inquiry

Background

GCH1 Gene Knockout Cell Lines are specialized biological reagents designed for the study and manipulation of the GTP cyclohydrolase 1 (GCH1) gene, a vital component in the biosynthesis of tetrahydrobiopterin (BH4), an essential cofactor in the metabolism of neurotransmitters. These cell lines are engineered to lack functional GCH1, facilitating the exploration of its biological roles and associated pathways in a controlled environment.

The key functions of these knockout cell lines stem from their ability to simulate the effects of GCH1 deficiency. By analyzing the resultant phenotypic changes, researchers can elucidate the consequences of BH4 depletion on cellular processes such as nitric oxide synthesis, dopamine metabolism, and other critical physiological pathways. The mechanistic insights gained from using GCH1 knockout models are invaluable for understanding the pathophysiology of diseases like hyperphenylalaninemia, as well as for assessing therapeutic strategies to restore normal BH4 levels.

The scientific importance of GCH1 Gene Knockout Cell Lines extends to various research and clinical applications, particularly in pharmacology, neurobiology, and genetic disorder research. They serve as cellular models that enable the study of potential treatments for conditions linked to BH4 deficiency and provide a platform for drug screening and development.

What sets our GCH1 Gene Knockout Cell Lines apart is their unparalleled specificity and reliability, achieved through rigorous validation processes. Compared to alternative models, these cell lines offer consistent reproducibility and versatility across diverse experimental setups. This high fidelity ensures that researchers can trust the outcomes of their studies, directly impacting the validity of their research findings.

Researchers, clinicians, and biopharmaceutical companies can derive significant value from our GCH1 Gene Knockout Cell Lines, as they represent a crucial tool for advancing studies aimed at addressing neurological and metabolic disorders. By employing these cell lines, users can foster breakthroughs that enhance therapeutic options and improve patient outcomes.

With our extensive expertise in genetic engineering and cellular biology, our company is committed to providing high-quality biological products that empower researchers and clinicians alike to progress their studies.

Please note that all services are for research use only. Not intended for any clinical use.

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