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SQSTM1 Knockout Cell Lines

Gene: SQSTM1

Official Full Name: sequestosome 1provided by HGNC

Gene Summary: This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone. [provided by RefSeq, Mar 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
GP00195 SQSTM1 gRNA3-gRNA4 KO plasmid SQSTM1 $850
GP00662 SQSTM1 gRNA5-gRNA6 KO plasmid SQSTM1 $850
KO00401 SQSTM1 Knockout cell line (HeLa) Human SQSTM1 1:3~1:6 Negative Online Inquiry
KO00402 SQSTM1 Knockout cell line (HCT 116) Human SQSTM1 1:2~1:4 Negative Online Inquiry
KO00629 SQSTM1 Knockout cell line (HEK293) Human SQSTM1 1:3~1:6 Negative Online Inquiry
KO00830 SQSTM1 Knockout cell line(Hep G2) Human SQSTM1 1:2~1:4 Negative Online Inquiry
KO00835 SQSTM1 Knockout cell line(BEAS-2B) Human SQSTM1 1:3~1:4 Negative Online Inquiry
KO00964 SQSTM1 Knockout cell line (HT-29) Human SQSTM1 1:2~1:4 Negative Online Inquiry
KO13744 SQSTM1 Knockout cell line (A549) Human SQSTM1 1:3~1:4 Negative Online Inquiry

Background

SQSTM1 Gene Knockout Cell Lines are specifically designed cellular models that have undergone targeted genetic modification to inactivate the SQSTM1 gene, which encodes the protein p62, a key regulator of various cellular processes including autophagy, oxidative stress response, and protein aggregation. By eliminating the expression of this gene, researchers can gain critical insights into its role in cellular homeostasis, signaling pathways, and its implications in diseases such as neurodegenerative disorders and cancer.

The key function of these knockout cell lines lies in their ability to mimic the physiological consequences of SQSTM1 gene depletion. This allows investigators to explore the modulation of autophagic processes and glycoprotein turnover without the influence of p62, thereby isolating its effects on cell function. The mechanism whereby the SQSTM1 gene contributes to cellular homeostasis involves the regulation of the NF-κB signaling pathway, as well as the selective degradation of ubiquitinated proteins, underscoring its role as a multifaceted adapter protein.

Scientifically, these cell lines are invaluable in the realm of research and clinical studies, providing a model for elucidating the molecular underpinnings of disorders that are associated with impaired autophagy and protein aggregation. They can serve as a platform for drug discovery and testing, enabling the development of therapeutics aimed at modulating autophagy pathways or targeting associated cellular dysfunctions. Compared to alternative models that may not fully replicate the loss of SQSTM1 function, these knockout cell lines provide a more precise tool for studying the pathophysiology of relevant diseases.

The unique selling points of the SQSTM1 Gene Knockout Cell Lines include their reliability, reproducibility, and the specificity of the knockout which eliminates confounding variables associated with off-target effects. This level of precision allows researchers and clinicians to draw more accurate conclusions from their experiments, ultimately leading to better applications of their findings in therapeutic contexts.

Choosing SQSTM1 Gene Knockout Cell Lines not only enhances the quality of experimental results but also empowers researchers with cutting-edge tools necessary to advance our understanding of complex biological systems. Our company prides itself on its extensive expertise in the development of innovative biological research products, ensuring that researchers have access to high-quality, validated models to support their scientific endeavors.

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

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