Gene: CC2D1A
Official Full Name: coiled-coil and C2 domain containing 1Aprovided by HGNC
Gene Summary: This gene encodes a transcriptional repressor that binds to a conserved 14-bp 5'-repressor element and regulates expression of the 5-hydroxytryptamine (serotonin) receptor 1A gene in neuronal cells. The DNA binding and transcriptional repressor activities of the protein are inhibited by calcium. A mutation in this gene results in a nonsyndromic form of cognitive disability (MRT3). [provided by RefSeq, Jul 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20572 | CC2D1A Knockout cell line (HeLa) | Human | CC2D1A | 1:3~1:6 | Negative | Online Inquiry |
KO20573 | CC2D1A Knockout cell line (HCT 116) | Human | CC2D1A | 1:2~1:4 | Negative | Online Inquiry |
KO20574 | CC2D1A Knockout cell line (HEK293) | Human | CC2D1A | 1:3~1:6 | Negative | Online Inquiry |
KO20575 | CC2D1A Knockout cell line (A549) | Human | CC2D1A | 1:3~1:4 | Negative | Online Inquiry |
CC2D1A Gene Knockout Cell Lines are sophisticated biological tools engineered to facilitate gene function studies by targeting the CC2D1A gene, which plays a critical role in cellular processes such as protein trafficking and synaptic function. These knockout cell lines are created using advanced CRISPR-Cas9 technology, effectively disrupting the CC2D1A gene to investigate its contributions to cellular behavior, disease mechanisms, and therapeutic responses.
The primary function of CC2D1A Gene Knockout Cell Lines lies in their ability to provide valuable insights into gene function by allowing researchers to study the phenotypic consequences of loss-of-function mutations. By utilizing these cell lines, scientists can elucidate pathways involved in neurodevelopment, neurodegenerative diseases, and other conditions where CC2D1A is implicated. The knockout model effectively mimics human disease scenarios, making it an essential tool in translational research.
The scientific importance of these cell lines extends to both academic and clinical contexts, where they aid in drug discovery, pathophysiological studies, and biomarker identification. Their precision in gene editing enables reliable data generation, which is crucial for high-stakes research projects and can ultimately guide clinical applications in targeted therapies.
One significant advantage of CC2D1A Gene Knockout Cell Lines is their higher specificity and efficiency compared to traditional methods, such as RNA interference or chemical inhibitors, which can exhibit off-target effects. These cell lines maintain stable genetic modifications, allowing for reproducible experimental outcomes that speed up research timelines and improve confidence in results.
For researchers and clinicians endeavoring to unravel the complexities of gene function and its implications in health, CC2D1A Gene Knockout Cell Lines represent a powerful asset. They not only contribute to foundational knowledge but also enhance the potential for innovative therapeutic developments. Our company prides itself on delivering high-quality, reliable biological products, leveraging state-of-the-art technologies to support advancements in life sciences and improve the research landscape.
Please note that all services are for research use only. Not intended for any clinical use.
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