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DERL1 Knockout Cell Lines

Gene: DERL1

Official Full Name: derlin 1provided by HGNC

Gene Summary: The protein encoded by this gene is a member of the derlin family. Members of this family participate in the ER-associated degradation response and retrotranslocate misfolded or unfolded proteins from the ER lumen to the cytosol for proteasomal degradation. This protein recognizes substrate in the ER and works in a complex to retrotranslocate it across the ER membrane into the cytosol. This protein may select cystic fibrosis transmembrane conductance regulator protein (CFTR) for degradation as well as unfolded proteins in Alzheimer's disease. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO01508 DERL1 Knockout cell line (HeLa) Human DERL1 1:3~1:6 Negative Online Inquiry
KO01509 DERL1 Knockout cell line (HCT 116) Human DERL1 1:2~1:4 Negative Online Inquiry
KO01510 DERL1 Knockout cell line (HEK293) Human DERL1 1:3~1:6 Negative Online Inquiry
KO01511 DERL1 Knockout cell line (A549) Human DERL1 1:3~1:4 Negative Online Inquiry

Background

DERL1 Gene Knockout Cell Lines are genetically modified cell lines that have been engineered to stably express a complete knockout of the DERL1 gene. This gene, associated with endoplasmic reticulum (ER) quality control and proteostasis, plays a vital role in cellular responses to stress, protein folding, and degradation pathways. By understanding the function of DERL1 through targeted gene knockout, researchers can gain insights into various cellular processes and diseases linked to protein misfolding and ER stress, such as neurodegenerative disorders and metabolic syndromes.

The mechanism behind the activity of DERL1 involves the regulation of the ER-associated degradation (ERAD) pathway, wherein misfolded or unassembled proteins are recognized and translocated for proteasomal degradation. The knockout of DERL1, therefore, allows for the assessment of its functional significance in maintaining cellular proteostasis and identifying the mechanistic underpinnings of diseases associated with ER dysfunction.

In research and clinical settings, these cell lines serve as essential tools in the investigation of cellular pathways and the performance of high-throughput drug screening assays targeting ER stress responses. The DERL1 knockout models facilitate the characterization of potential therapeutic interventions and novel drug targets, providing vital insights into treatment strategies for diseases orchestrated by ER stress and dysregulated protein homeostasis.

What distinguishes Derl1 Gene Knockout Cell Lines from alternative models is their robust, stable genetic modification, which ensures reproducibility and reliability in experimental results. The specificity of the knockout enhances the precision of the data obtained, allowing for more accurate interpretations of the results.

For researchers and clinicians, leveraging DERL1 Gene Knockout Cell Lines represents an invaluable opportunity to advance understanding of fundamental biological processes and contribute to the development of innovative therapies. Our company specializes in providing high-quality, genetically modified cell lines, underpinned by years of expertise in cellular biology, to drive forward the frontiers of scientific discovery.

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

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