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SESN1 Knockout Cell Lines

Gene: SESN1

Official Full Name: sestrin 1provided by HGNC

Gene Summary: This gene encodes a member of the sestrin family. Sestrins are induced by the p53 tumor suppressor protein and play a role in the cellular response to DNA damage and oxidative stress. The encoded protein mediates p53 inhibition of cell growth by activating AMP-activated protein kinase, which results in the inhibition of the mammalian target of rapamycin protein. The encoded protein also plays a critical role in antioxidant defense by regenerating overoxidized peroxiredoxins, and the expression of this gene is a potential marker for exposure to radiation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO27728 SESN1 Knockout cell line (HeLa) Human SESN1 1:3~1:6 Negative Online Inquiry
KO27729 SESN1 Knockout cell line (HCT 116) Human SESN1 1:2~1:4 Negative Online Inquiry
KO27730 SESN1 Knockout cell line (HEK293) Human SESN1 1:3~1:6 Negative Online Inquiry
KO27731 SESN1 Knockout cell line (A549) Human SESN1 1:3~1:4 Negative Online Inquiry

Background

SESN1 Gene Knockout Cell Lines are specialized cellular models engineered to lack the expression of the SESN1 gene, which encodes the protein sestrin 1, a critical regulator of cellular stress responses. These knockout cell lines serve as invaluable tools for studying the fundamental roles of SESN1 in various physiological processes, including autophagy, oxidative stress response, and metabolic regulation. The absence of SESN1 allows researchers to explore the gene's involvement in cellular signaling pathways and its implications in conditions such as cancer, neurodegenerative diseases, and metabolic syndromes.

The key functionality of SESN1 Gene Knockout Cell Lines lies in their ability to mimic disease states and facilitate mechanistic studies that reveal the intricate roles of SESN1 in cellular homeostasis. By utilizing advanced CRISPR/Cas9 genome editing technology, these cell lines provide consistent and reproducible results, allowing for efficient validation of hypotheses regarding the SESN1 pathway. The knockout phenotype enables researchers to dissect the signaling cascades modulated by SESN1, thereby accelerating the discovery of potential therapeutic targets.

From a scientific standpoint, SESN1 Gene Knockout Cell Lines are essential for understanding the biological impact of SESN1 deletion in both in vitro and in vivo models. Their relevance extends to clinical research, where insights gained can guide the development of novel interventions for diseases characterized by SESN1 dysregulation.

What sets these cell lines apart from traditional models is their precise genetic modification and improved reliability in experimental outcomes. This specificity significantly enhances the interpretation of data and reduces the variability often associated with other models. Researchers and clinicians will find these knockout cell lines particularly valuable as they seek to elucidate pathways involving cell survival, aging, and stress tolerance.

With a commitment to advancing biological research, our company leverages a team of experts in genetic engineering and cell biology to deliver high-quality products like SESN1 Gene Knockout Cell Lines. Our dedication to innovation ensures that we provide cutting-edge tools that empower researchers to push the boundaries of knowledge and therapeutic development.

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

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