Gene: KIAA0319
Official Full Name: KIAA0319provided by HGNC
Gene Summary: This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in this gene are associated with dyslexia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO32638 | KIAA0319 Knockout cell line (HeLa) | Human | KIAA0319 | 1:3~1:6 | Negative | Online Inquiry |
KO32639 | KIAA0319 Knockout cell line (HCT 116) | Human | KIAA0319 | 1:2~1:4 | Negative | Online Inquiry |
KO32640 | KIAA0319 Knockout cell line (HEK293) | Human | KIAA0319 | 1:3~1:6 | Negative | Online Inquiry |
KO32641 | KIAA0319 Knockout cell line (A549) | Human | KIAA0319 | 1:3~1:4 | Negative | Online Inquiry |
KIAA0319 gene knockout cell lines are genetically engineered cell lines that have undergone the targeted disruption of the KIAA0319 gene, which is implicated in language and reading abilities. These cell lines serve as a model system for researchers investigating the molecular mechanisms of neurodevelopmental disorders, particularly those associated with dyslexia, as mutations or variations in the KIAA0319 gene have been correlated with altered cognitive abilities in humans.
The key functions of KIAA0319 involve its role in neuronal development and synaptic plasticity, which are crucial processes for cognitive function. By disrupting the KIAA0319 gene within these cell lines, researchers can elucidate its specific contributions to neurodevelopment, explore downstream signaling pathways, and assess the impact on neuronal morphology and function. This controlled environment allows for the manipulation of various experimental conditions, enabling scientists to study the gene's role in a systematic manner.
The scientific importance of KIAA0319 gene knockout cell lines is significant in both research and clinical settings. They provide researchers with a powerful tool to investigate the genetic and environmental factors influencing language processing and literacy. Moreover, they have potential applications in drug screening and therapeutic interventions aimed at ameliorating dyslexia and related cognitive disorders. With growing interest in personalized medicine, the insights gained from these models can inform strategies tailored to individual therapeutic needs.
Unlike traditional wild-type cell lines, KIAA0319 knockout cell lines offer a unique advantage by presenting a focused approach to studying specific genetic contributions to disease. Their specificity allows for a deeper understanding of the subtle mechanisms at play, which can lead to innovative treatment strategies. Additionally, the ability to replicate human genetic conditions in vitro positions these cell lines as an essential resource for both academic and commercial research.
Researchers and clinicians will find significant value in these knockout cell lines due to their capacity to mimic the human genetic background of specific disorders. This precision enables high-throughput screening and targeted experimental designs that could accelerate the discovery of effective interventions.
Our company is dedicated to providing high-quality biological products and support for researchers, underscoring our commitment to advancing scientific understanding in areas critical to human health. With our KIAA0319 gene knockout cell lines, we empower scientists to delve deeper into the complexities of neurodevelopmental disorders, paving the way for future breakthroughs in diagnosis and treatment.
Please note that all services are for research use only. Not intended for any clinical use.
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