Gene: ATN1
Official Full Name: atrophin 1provided by HGNC
Gene Summary: Dentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion from 7-35 copies to 49-93 copies of a trinucleotide repeat (CAG/CAA) within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein. [provided by RefSeq, Jul 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO06091 | ATN1 Knockout cell line (HeLa) | Human | ATN1 | 1:3~1:6 | Negative | Online Inquiry |
KO06092 | ATN1 Knockout cell line (HCT 116) | Human | ATN1 | 1:2~1:4 | Negative | Online Inquiry |
KO06093 | ATN1 Knockout cell line (HEK293) | Human | ATN1 | 1:3~1:6 | Negative | Online Inquiry |
KO06094 | ATN1 Knockout cell line (A549) | Human | ATN1 | 1:3~1:4 | Negative | Online Inquiry |
ATN1 Gene Knockout Cell Lines are genetically engineered cellular models designed to facilitate the study of the ATN1 gene's function and its role in various biological processes. By employing CRISPR-Cas9 technology, these cell lines allow for the precise knockout of the ATN1 gene, providing researchers with invaluable tools to explore the genetic underpinnings of related diseases, particularly those linked to neurodegenerative disorders such as Spinocerebellar Ataxia Type 1 (SCA1).
The key function of the ATN1 Gene Knockout Cell Lines lies in their ability to mimic the pathological features associated with ATN1 gene disruption. In these cell lines, the absence of the ATN1 protein serves as a model for analyzing cellular responses, signaling pathways, and gene expression alterations that occur as a result of this genetic modification. Mechanistically, these knockouts help shed light on how the misregulation of the ATN1 gene leads to neurodegeneration and related phenotypes.
The scientific importance of these cell lines extends beyond basic research; they serve as critical tools for drug discovery and development. By utilizing ATN1 Gene Knockout Cell Lines, researchers can screen therapeutic compounds that may restore normal cellular function or mitigate disease progression, ultimately guiding the development of potential treatment strategies in clinical settings.
A unique advantage of the ATN1 Gene Knockout Cell Lines over conventional models is their specificity and accuracy, drastically reducing off-target effects commonly seen with less precise genetic modification techniques. Additionally, these cell lines are characterized by high reproducibility and scalability, making them suitable for high-throughput screening applications.
Researchers, clinicians, and pharmaceutical companies can derive substantial value from these cell lines, as they create opportunities to uncover novel insights and design effective interventions for ATN1-associated conditions.
Our commitment to advancing biological research is reflected in our expertise in high-quality genetic models, including the ATN1 Gene Knockout Cell Lines, which are meticulously developed to empower scientific discovery and innovation in the study of genetic diseases.
Please note that all services are for research use only. Not intended for any clinical use.
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