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ATL1 Knockout Cell Lines

Gene: ATL1

Official Full Name: atlastin GTPase 1provided by HGNC

Gene Summary: The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO23129 ATL1 Knockout cell line (HeLa) Human ATL1 1:3~1:6 Negative Online Inquiry
KO23130 ATL1 Knockout cell line (HCT 116) Human ATL1 1:2~1:4 Negative Online Inquiry
KO23131 ATL1 Knockout cell line (HEK293) Human ATL1 1:3~1:6 Negative Online Inquiry
KO23132 ATL1 Knockout cell line (A549) Human ATL1 1:3~1:4 Negative Online Inquiry

Background

ATL1 Gene Knockout Cell Lines are engineered cellular models specifically designed to study the functions and implications of the ATL1 gene, which plays a crucial role in various cellular processes, particularly in the context of hereditary spastic paraplegia (HSP). By utilizing CRISPR/Cas9 technology, these cell lines exhibit a complete knockout of the ATL1 gene, enabling researchers to investigate the resulting phenotypic effects and underlying molecular mechanisms associated with ATL1 loss-of-function mutations.

The primary function of ATL1 involves maintaining the integrity of the cellular cytoskeleton and modulating intracellular transport processes. In the absence of ATL1, these knockout cell lines undergo distinct morphological changes and altered signaling pathways, offering insights into neurodegenerative mechanisms and potential therapeutic targets. This unique functionality makes ATL1 Gene Knockout Cell Lines invaluable for advancing our understanding of genetic disorders linked to mitochondrial dysfunction, as well as their impacts on neuronal health and development.

Scientifically, the applications of ATL1 Gene Knockout Cell Lines extend to both fundamental research and clinical settings. Researchers can use these models to explore pathways involved in cellular stress responses, investigate drug targets, and conduct high-throughput screening for compounds that may restore normal function in ATL1-deficient cells. The potential to elucidate the role of ATL1 gene depletion in disease etiology underlines the importance of this product, as findings derived from these studies can contribute significantly to the development of therapeutic strategies for HSP and related disorders.

What sets ATL1 Gene Knockout Cell Lines apart from alternative cellular models is their precise gene editing, which leads to a complete ablation of the gene of interest, ensuring a robust and reproducible research environment. Furthermore, these cell lines are developed using state-of-the-art techniques, ensuring genomic integrity and compliance with research safety standards.

For researchers and clinicians dedicated to neurobiology or genetic disorders, ATL1 Gene Knockout Cell Lines offer a valuable platform that bridges basic science with clinical application. They enable user-driven inquiries that can translate findings into meaningful advances in treatment options.

As a leader in providing innovative biological products, our company is committed to equipping the scientific community with high-quality, reliable tools for cutting-edge research. With an emphasis on precision and reproducibility, we aim to facilitate discoveries that can ultimately improve patient outcomes.

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

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