Gene: ATP10A
Official Full Name: ATPase phospholipid transporting 10A (putative)provided by HGNC
Gene Summary: The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. This gene is maternally expressed. It maps within the most common interval of deletion responsible for Angelman syndrome, also known as 'happy puppet syndrome'. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20849 | ATP10A Knockout cell line (A549) | Human | ATP10A | 1:3~1:4 | Negative | Online Inquiry |
ATP10A Gene Knockout Cell Lines are precision-engineered cellular models that have been optimized to selectively disable the ATP10A gene, which encodes a member of the P4-ATPase family of proteins responsible for phospholipid transport across cellular membranes. These knockout cell lines illustrate the functionality of ATP10A and allow researchers to investigate its role in cellular processes, such as lipid metabolism, autophagy, and disease pathogenesis, including cancer and neurodegenerative disorders.
The key functionality of ATP10A Gene Knockout Cell Lines lies in their ability to simulate the loss-of-function conditions observed in various pathological states. By utilizing CRISPR-Cas9 gene-editing technology, these cell lines enable researchers to accurately dissect the molecular mechanisms that govern ATP10A-related activities within different biological contexts. This allows for a high-resolution exploration of how disruptions in lipid homeostasis can lead to dysregulations in cell signaling and metabolic pathways.
The scientific importance of ATP10A Gene Knockout Cell Lines extends to both research and clinical applications. In research, they are invaluable for elucidating the molecular underpinnings of diseases associated with ATP10A dysfunction, providing insights that could lead to novel therapeutic strategies. Clinically, these models can assist in drug discovery and development pipelines, evaluating pharmacological efficacy and safety in conditions pertaining to lipid metabolism and cellular dysfunction.
Compared to traditional wild-type cell lines, ATP10A Gene Knockout Cell Lines offer specific advantages, including enhanced experimental reproducibility, reduced variability, and the ability to study gene function with precision. This makes them particularly appealing to researchers seeking in-depth mechanistic insights and consistent results across experimental replicates.
For researchers and clinicians, the value of ATP10A Gene Knockout Cell Lines extends beyond mere utility; they represent a cutting-edge tool in the quest to understand complex biological systems. Their deployment can significantly accelerate the pathway from bench to bedside, facilitating discoveries that may translate into pioneering treatments for debilitating diseases.
At our company, we are committed to advancing scientific research by providing high-quality biological products designed to meet the evolving needs of the scientific community. With a focus on precision and innovation, our ATP10A Gene Knockout Cell Lines exemplify our dedication to fostering advancements in biomedical research.
Please note that all services are for research use only. Not intended for any clinical use.
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