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ASS1 Knockout Cell Lines

Gene: ASS1

Official Full Name: argininosuccinate synthase 1provided by HGNC

Gene Summary: The protein encoded by this gene catalyzes the penultimate step of the arginine biosynthetic pathway. There are approximately 10 to 14 copies of this gene including the pseudogenes scattered across the human genome, among which the one located on chromosome 9 appears to be the only functional gene for argininosuccinate synthetase. Mutations in the chromosome 9 copy of this gene cause citrullinemia. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00975 ASS1 Knockout cell line (HCT 116) Human ASS1 Negative Online Inquiry
KO38892 ASS1 Knockout cell line (HeLa) Human ASS1 1:3~1:6 Negative Online Inquiry
KO38893 ASS1 Knockout cell line (HEK293) Human ASS1 1:3~1:6 Negative Online Inquiry
KO38894 ASS1 Knockout cell line (A549) Human ASS1 1:3~1:4 Negative Online Inquiry

Background

ASS1 Gene Knockout Cell Lines are specialized cellular models in which the argininosuccinate synthetase 1 (ASS1) gene has been genetically disrupted, enabling researchers to study various biological processes relating to arginine metabolism and nitrogen balance. These cell lines play a critical role in advancing our understanding of specific metabolic pathways associated with disorders such as argininemia and other related urea cycle disorders, thus providing a valuable tool for both basic research and therapeutic development.

Key functions of ASS1 gene knockout cell lines involve the study of cellular responses to altered arginine availability and the impact on nitrogen metabolism. By examining these cellular models, researchers can elucidate the pathways leading to metabolic dysregulation and explore the potential therapeutic avenues for conditions where ASS1 is implicated. The absence of functional ASS1 allows for the examination of compensatory mechanisms within the urea cycle, as well as the effects on cell proliferation, apoptosis, and overall cellular health, providing rich insights into metabolic disease states.

The scientific importance of these cell lines extends to applications in drug screening, gene therapy research, and biotechnology. They can be used to evaluate the efficacy of therapeutic compounds designed to restore arginine levels or mitigate the effects of arginine deficiency. In clinical settings, such models assist in identifying biomarkers for the diagnosis and treatment of metabolic disorders, enhancing translational research.

Compared to traditional cell lines, ASS1 gene knockout models offer a unique advantage by providing a targeted approach to studying specific metabolic pathways associated with this gene. Their precise genetic modification allows for more accurate modeling of human diseases, which can lead to more effective treatment strategies. Additionally, the customized nature of these cell lines enables researchers to explore the unique biological features that result from the complete absence of ASS1, providing insights that other non-specific models may not.

The value of ASS1 Gene Knockout Cell Lines lies in their ability to bridge the gap between basic biological research and clinical applications, making them indispensable for researchers and clinicians focused on metabolic disorders. Our company is dedicated to providing high-quality biological research tools, backed by extensive expertise in genetic engineering and cell biology, ensuring that our customers have access to the best resources for their research needs.

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

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