Gene: ATP8A1
Official Full Name: ATPase phospholipid transporting 8A1provided by HGNC
Gene Summary: The P-type adenosinetriphosphatases (P-type ATPases) are a family of proteins which use the free energy of ATP hydrolysis to drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily catalyzes transport of heavy metal ions. Another subfamily transports non-heavy metal ions (NMHI). The protein encoded by this gene is a member of the third subfamily of P-type ATPases and acts to transport amphipaths, such as phosphatidylserine. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO31916 | ATP8A1 Knockout cell line (HeLa) | Human | ATP8A1 | 1:3~1:6 | Negative | Online Inquiry |
KO31917 | ATP8A1 Knockout cell line (HCT 116) | Human | ATP8A1 | 1:2~1:4 | Negative | Online Inquiry |
KO31918 | ATP8A1 Knockout cell line (HEK293) | Human | ATP8A1 | 1:3~1:6 | Negative | Online Inquiry |
ATP8A1 Gene Knockout Cell Lines are engineered cell lines that have had the ATP8A1 gene specifically disrupted or knocked out, allowing researchers to investigate the gene's role in various biological processes. The ATP8A1 gene encodes a member of the P-type ATPase family, which is crucial in maintaining cellular ion balance and lipid asymmetry in membranes. By utilizing these knockout cell lines, scientists can unravel the effects of ATP8A1 deficiency on cellular functions, such as membrane trafficking, apoptosis, and signal transduction pathways.
The primary mechanism by which these cell lines function is through the absence of the ATP8A1 protein, enabling researchers to study the resultant phenotypic changes and molecular mechanisms underlying specific diseases or cellular anomalies. For instance, the loss of ATP8A1 has been implicated in several neurodegenerative conditions, making these cell lines invaluable for exploring therapeutic strategies or potential biomarkers.
In terms of scientific importance, ATP8A1 Gene Knockout Cell Lines are pivotal in both fundamental research and clinical applications. They serve as powerful tools in drug discovery, genetic studies, and the development of targeted therapies by providing insights into the pathophysiological roles of ATP8A1. Researchers can utilize these lines to assess drug efficacy, elucidate disease mechanisms, and evaluate genetic interactions under controlled conditions.
One key advantage of ATP8A1 Gene Knockout Cell Lines over traditional methods is their ability to provide consistent, reproducible results, as they eliminate genetic variability found in primary cultures or animal models. Furthermore, these cell lines are readily accessible and allow for high-throughput screening, which can significantly expedite research timelines.
The value of ATP8A1 Gene Knockout Cell Lines cannot be overstated; they equip researchers and clinicians with the tools necessary to drive advancements in understanding and treating diseases associated with ATP8A1 dysfunction. These versatile cell lines open up new avenues for discovery, enabling a deeper understanding of the complex interplay between genes and diseases.
Our company is dedicated to advancing scientific research by providing high-quality, meticulously validated biological products such as ATP8A1 Gene Knockout Cell Lines. With extensive expertise in genetic engineering and cell line development, we offer innovative solutions that empower researchers to push the boundaries of discovery in molecular biology and therapeutic development.
Please note that all services are for research use only. Not intended for any clinical use.
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