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ULK1 Knockout Cell Lines

Gene: ULK1

Official Full Name: unc-51 like autophagy activating kinase 1provided by HGNC

Gene Summary: Enables identical protein binding activity; protein serine/threonine kinase activity; and small GTPase binding activity. Involved in several processes, including protein phosphorylation; regulation of autophagy; and regulation of protein lipidation. Located in bounding membrane of organelle; cytosol; and phagophore assembly site membrane. Part of Atg1/ULK1 kinase complex and phagophore assembly site. Is active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00089 ULK1 Knockout cell line (U-2 OS) Human ULK1 1:3~1:5 Negative Online Inquiry
KO00226 ULK1 Knockout cell line (HCT 116) Human ULK1 1:2~1:4 Negative Online Inquiry
KO00227 ULK1 Knockout cell line (A549) Human ULK1 1:3~1:4 Negative Online Inquiry
KO09141 ULK1 Knockout cell line (HeLa) Human ULK1 1:3~1:6 Negative Online Inquiry
KO09142 ULK1 Knockout cell line (HEK293) Human ULK1 1:3~1:6 Negative Online Inquiry

Background

ULK1 Gene Knockout Cell Lines are genetically engineered cell models that specifically have the ULK1 (Unc-51 Like Autophagy Activating Kinase 1) gene disrupted or deleted. This product is vital for studying the role of ULK1 in various physiological and pathological processes, particularly in autophagy, a critical cellular degradation pathway that maintains cellular homeostasis. The ULK1 kinase is an essential initiator of autophagy, and its functional loss in these knockout cell lines provides insights into the mechanisms by which autophagy contributes to cell survival, stress response, and metabolism.

The key function of ULK1 Gene Knockout Cell Lines lies in their ability to serve as a powerful tool for investigating the impact of ULK1 loss on cellular processes. By disrupting ULK1 activity, researchers can observe changes in autophagic flux, metabolic pathways, and responses to nutrient deprivation or stress. These knockouts facilitate the exploration of ULK1's interactions with other signaling pathways, thereby supporting the identification of potential therapeutic targets for diseases where autophagy is dysregulated, such as cancer, neurodegeneration, and metabolic disorders.

The scientific importance of ULK1 Gene Knockout Cell Lines extends into both research and clinical settings, providing unparalleled advantages over other experimental models. The precise gene editing through technologies such as CRISPR-Cas9 ensures high specificity in gene disruption, thereby reducing off-target effects commonly seen in other methods. These cell lines allow for reproducible experimentation, which is crucial for validating findings and providing reliable data for publication.

One of the unique selling points of our ULK1 Gene Knockout Cell Lines is the ability to use these models in various cell types, including cancerous and non-cancerous tissues, enhancing the versatility and applicability of research outcomes. Additionally, their utility in high-throughput screening environments is significant, allowing for the efficient evaluation of pharmacological interventions that may modulate autophagy.

For researchers and clinicians focused on elucidating the complex roles of ULK1 in health and disease, these knockout cell lines represent a valuable resource. They enable more accurate modeling of diseases associated with autophagy dysfunction, paving the way for innovative treatment strategies and drug discovery.

Our company is committed to advancing biological research through high-quality, precisely engineered products. With extensive expertise in genetic engineering and a dedication to scientific excellence, we provide researchers with the tools necessary to advance their understanding of cellular mechanisms, ultimately contributing to breakthroughs in biomedical science.

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

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