Gene: SMG9
Official Full Name: SMG9 nonsense mediated mRNA decay factorprovided by HGNC
Gene Summary: This gene encodes a regulatory subunit of the SMG1 complex, which plays a critical role in nonsense-mediated mRNA decay (NMD). Binding of the encoded protein to the SMG1 complex kinase scaffold protein results in the inhibition of its kinase activity. Mutations in this gene cause a multiple congenital anomaly syndrome in human patients, characterized by brain malformation, congenital heart disease and other features. [provided by RefSeq, Jul 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO13938 | SMG9 Knockout cell line (HeLa) | Human | SMG9 | 1:3~1:6 | Negative | Online Inquiry |
KO13939 | SMG9 Knockout cell line (HCT 116) | Human | SMG9 | 1:2~1:4 | Negative | Online Inquiry |
KO13940 | SMG9 Knockout cell line (HEK293) | Human | SMG9 | 1:3~1:6 | Negative | Online Inquiry |
KO13941 | SMG9 Knockout cell line (A549) | Human | SMG9 | 1:3~1:4 | Negative | Online Inquiry |
SMG9 Gene Knockout Cell Lines are highly specialized mammalian cell lines that have been genetically engineered to lack the expression of the SMG9 gene. This product allows researchers to study the functional impacts of SMG9 deficiency, particularly in the context of mRNA surveillance and nonsense-mediated decay (NMD) pathways. By utilizing these knockout cell lines, scientists can observe and dissect the role of SMG9 in gene expression regulation and its influence on cellular responses to stress signals, which are fundamental areas of interest in molecular biology.
The SMG9 gene is known for its role in the NMD pathway, a critical cellular mechanism responsible for the degradation of mRNAs containing premature stop codons, thereby preventing the synthesis of truncated and potentially deleterious proteins. The key functions of the SMG9 Gene Knockout Cell Lines allow researchers to investigate the consequences of disrupted NMD, including altered protein levels, cellular stress responses, and changes in signaling pathways. By isolating the effects of the SMG9 absence, researchers can gain insights that have implications ranging from basic cellular biology to therapeutic strategies for diseases associated with mRNA processing anomalies.
In research and clinical settings, the value of SMG9 Gene Knockout Cell Lines is further underscored by their potential applications in drug discovery, gene therapy, and understanding genetic disorders. These cell lines provide a robust model to explore how defects in NMD contribute to various pathologies, enabling researchers to develop targeted interventions. Compared to traditional models, such as wild-type cell lines or those altered by transient methods, these knockout cell lines offer a stable, long-lasting platform for experimentation and reproducibility, which is essential for advancing scientific inquiry.
Moreover, the ability to elucidate the specific action of SMG9 in cellular contexts positions this product as a powerful tool for elucidating mechanistic pathways involved in human health and disease. Researchers and clinicians can benefit from a greater understanding of disease mechanisms and pave the way for novel therapeutic approaches.
Our company has extensive expertise in the production and characterization of genetically engineered cell lines, ensuring our SMG9 Gene Knockout Cell Lines meet the highest standards of quality and reliability. With our commitment to advancing biological research, we stand ready to support your studies with innovative tools tailored to your specific needs.
Please note that all services are for research use only. Not intended for any clinical use.
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