Gene: SIL1
Official Full Name: SIL1 nucleotide exchange factorprovided by HGNC
Gene Summary: This gene encodes a resident endoplasmic reticulum (ER), N-linked glycoprotein with an N-terminal ER targeting sequence, 2 putative N-glycosylation sites, and a C-terminal ER retention signal. This protein functions as a nucleotide exchange factor for another unfolded protein response protein. Mutations in this gene have been associated with Marinesco-Sjogren syndrome. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20418 | SIL1 Knockout cell line (HeLa) | Human | SIL1 | 1:3~1:6 | Negative | Online Inquiry |
KO20419 | SIL1 Knockout cell line (HCT 116) | Human | SIL1 | 1:2~1:4 | Negative | Online Inquiry |
KO20420 | SIL1 Knockout cell line (HEK293) | Human | SIL1 | 1:3~1:6 | Negative | Online Inquiry |
KO20421 | SIL1 Knockout cell line (A549) | Human | SIL1 | 1:3~1:4 | Negative | Online Inquiry |
SIL1 Gene Knockout Cell Lines are specifically engineered cellular models created to study the functional implications of the SIL1 gene, which encodes a co-chaperone involved in protein folding and mitochondrial function. By utilizing CRISPR/Cas9 gene editing technology, these cell lines enable researchers to investigate the biochemical pathways affected by the absence of SIL1, thereby illuminating its role in cellular stress responses and mitochondrial dynamics.
The primary function of SIL1 involves its contribution to the maturation of mitochondrial chaperones, including those required for proper protein assembly within the mitochondria. When SIL1 is knocked out, cells exhibit an accumulation of unfolded proteins and increased susceptibility to oxidative stress, providing invaluable insights into diseases linked to mitochondrial dysfunction, such as neurodegenerative disorders and certain cancers. By elucidating the mechanistic pathways that rely on SIL1, researchers can better understand disease etiology and identify potential therapeutic targets.
The scientific importance of SIL1 Gene Knockout Cell Lines lies in their application across various research domains, from basic cellular biology to clinical therapeutic development. These models offer a reliable platform for screening drug efficacy and understanding genetic factors that influence disease states associated with mitochondrial anomalies.
Compared to other knockout models, SIL1 cell lines stand out due to their precise gene editing, ensuring a complete loss of function and reproducibility in experimental results. This specificity and reliability decrease variability and increase confidence in experimental outcomes.
For researchers and clinicians alike, the availability of SIL1 Gene Knockout Cell Lines provides a unique opportunity to bridge fundamental research and clinical applications. Understanding the implications of SIL1’s function can lead directly to advancements in treatment strategies for diseases characterized by mitochondrial dysregulation.
With a strong background in genetic engineering and a commitment to providing high-quality research tools, our company is poised to assist the scientific community in advancing knowledge and therapeutic approaches surrounding mitochondrial diseases through SIL1 Gene Knockout Cell Lines.
Please note that all services are for research use only. Not intended for any clinical use.
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