Gene: SEL1L
Official Full Name: SEL1L adaptor subunit of SYVN1 ubiquitin ligaseprovided by HGNC
Gene Summary: The protein encoded by this gene is part of a protein complex required for the retrotranslocation or dislocation of misfolded proteins from the endoplasmic reticulum lumen to the cytosol, where they are degraded by the proteasome in a ubiquitin-dependent manner. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00062 | SEL1L Knockout cell line (Hep G2) | Human | SEL1L | Negative | Online Inquiry | |
KO01800 | SEL1L Knockout cell line (HeLa) | Human | SEL1L | 1:3~1:6 | Negative | Online Inquiry |
KO01801 | SEL1L Knockout cell line (HCT 116) | Human | SEL1L | 1:2~1:4 | Negative | Online Inquiry |
KO01802 | SEL1L Knockout cell line (HEK293) | Human | SEL1L | 1:3~1:6 | Negative | Online Inquiry |
KO01803 | SEL1L Knockout cell line (A549) | Human | SEL1L | 1:3~1:4 | Negative | Online Inquiry |
SEL1L Gene Knockout Cell Lines are genetically engineered cell lines where the SEL1L gene has been inactivated using advanced CRISPR-Cas9 technology. This knockout results in the disruption of the cellular mechanisms associated with protein quality control and endoplasmic reticulum (ER) stress response, allowing researchers to study the downstream effects of SEL1L deficiency. The key function of these cell lines lies in their ability to serve as a vital tool for understanding the implications of SEL1L in health and disease, particularly its role in neurodegeneration, inflammation, and cancer.
Mechanistically, SEL1L encodes a protein that is integral to the ER-associated degradation (ERAD) pathway, which is crucial for maintaining cellular homeostasis by ensuring the proper turnover of misfolded proteins. By utilizing these knockout cell lines, scientists can delve into the pathophysiological outcomes resulting from impaired SEL1L function, enabling the exploration of novel therapeutic targets and strategies in clinical research domains.
The scientific importance of SEL1L Gene Knockout Cell Lines is underscored by their applications in studying a variety of diseases, including neurodegenerative disorders and metabolic syndrome, where ER stress is implicated. Additionally, these cell lines can be employed in drug discovery to evaluate the efficacy and safety of small molecules targeting related pathways, making them invaluable in translational research settings.
One significant advantage of our SEL1L Gene Knockout Cell Lines is their high specificity and reproducibility compared to traditional models that may have background variations in endogenous SEL1L expression. Furthermore, they offer a versatile platform that can be used in various assays, including functional studies, proliferation assays, and high-throughput screening.
For researchers and clinicians, the value of using SEL1L Gene Knockout Cell Lines lies in their potential to unravel the complexities of molecular biology and pathogenesis with precise genetic manipulation. They empower users with the ability to construct more reliable models that reflect the nuances of human diseases, ultimately driving innovation in the discovery of effective interventions.
Our company prides itself on its expertise in generating cutting-edge biological products, ensuring the highest quality standards for reliable results in research and clinical applications. By choosing our SEL1L Gene Knockout Cell Lines, users are equipped with a powerful tool that enhances their research capabilities and contributes to groundbreaking scientific discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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