Gene: ATP2B4
Official Full Name: ATPase plasma membrane Ca2+ transporting 4provided by HGNC
Gene Summary: The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 4. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO08138 | ATP2B4 Knockout cell line (HeLa) | Human | ATP2B4 | 1:3~1:6 | Negative | Online Inquiry |
KO08139 | ATP2B4 Knockout cell line (HCT 116) | Human | ATP2B4 | 1:2~1:4 | Negative | Online Inquiry |
KO08140 | ATP2B4 Knockout cell line (HEK293) | Human | ATP2B4 | 1:3~1:6 | Negative | Online Inquiry |
KO08141 | ATP2B4 Knockout cell line (A549) | Human | ATP2B4 | 1:3~1:4 | Negative | Online Inquiry |
ATP2B4 Gene Knockout Cell Lines are engineered cellular models specifically designed to lack the expression of the ATP2B4 gene, which encodes a calcium pump responsible for maintaining intracellular calcium homeostasis. These cell lines serve as a vital research tool for investigating the physiological roles of the ATP2B4 gene and its implications in various pathophysiological processes. By utilizing CRISPR-Cas9 or other gene-editing technologies, the knockout mechanism induces targeted mutations that effectively ablate ATP2B4 function, allowing researchers to elucidate its contributions to cellular signaling pathways, muscle contraction, and overall cellular physiology.
The key functions of these knockout cell lines lie in their ability to simulate pathological conditions that arise from disrupted calcium signaling. Researchers can employ these cell lines to conduct detailed studies into disorders such as cardiovascular diseases, muscular dystrophies, and neurodegenerative disorders, where calcium dysregulation is often implicated. The insights garnered from these models have the potential to revolutionize our understanding of these conditions, paving the way for novel therapeutic interventions.
In comparison to traditional cell models, ATP2B4 Gene Knockout Cell Lines provide a more precise and reliable framework for studying the specific contributions of the ATP2B4 gene. They allow for targeted investigation without the confounding effects present in whole-organism studies or less specific genetic modifications. Furthermore, these cell lines can be readily adapted for high-throughput screening applications, facilitating the discovery of small molecules or biological compounds that may restore normal ATP2B4 functions.
For researchers and clinicians, the value of ATP2B4 Gene Knockout Cell Lines extends beyond academic curiosity; they play an essential role in the translational research landscape by providing clearer insights into disease mechanisms and aiding the development of targeted therapies. By investing in these innovative cell lines, users gain access to a platform that drives significant advances in scientific knowledge and therapeutic discovery.
Our company is committed to excellence in the production of high-quality, genetically modified cell lines, ensuring that our products adhere to rigorous scientific standards and meet the diverse needs of researchers across various biological disciplines.
Please note that all services are for research use only. Not intended for any clinical use.
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