Gene: CNGA1
Official Full Name: cyclic nucleotide gated channel subunit alpha 1provided by HGNC
Gene Summary: The protein encoded by this gene is involved in phototransduction. Along with another protein, the encoded protein forms a cGMP-gated cation channel in the plasma membrane, allowing depolarization of rod photoreceptors. This represents the last step in the phototransduction pathway. Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease. Multiple transcript variants have been found for this gene. [provided by RefSeq, Oct 2019]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO07575 | CNGA1 Knockout cell line (HCT 116) | Human | CNGA1 | 1:2~1:4 | Negative | Online Inquiry |
CNGA1 Gene Knockout Cell Lines are specialized cellular models engineered to lack the expression of the CNGA1 gene, which encodes for the cyclic nucleotide phosphodiesterase-1 (CNG) channel alpha subunit—a critical component of phototransduction in retinal photoreceptors. These cell lines serve as vital tools for investigating the pathways and processes that rely on the proper functioning of the CNGA1 gene, especially in the context of visual signal transduction and retinal diseases.
The primary function of these knockout cell lines is to provide a controlled environment for studying the effects of CNGA1 absence on cellular physiology, signaling pathways, and gene expression profiles. By utilizing CRISPR-Cas9 technology or similar genome editing techniques, researchers can analyze downstream effects and compensatory mechanisms that occur in the absence of CNGA1, thus shedding light on its role in cellular function and disease pathology.
The scientific importance of CNGA1 Gene Knockout Cell Lines extends to both basic research and clinical applications. They enable researchers to model retinal degenerative diseases and to screen for potential therapeutic compounds that target aberrant signaling pathways. Additionally, these models can be instrumental in studying the functional consequences of CNGA1 mutations in human disorders, enhancing our understanding of genetics and ocular health.
What sets these knockout cell lines apart from traditional models is their specificity and precision; researchers effectively eliminate confounding factors associated with wild-type cells. The ability to discern the precise role of CNGA1's absence allows for more robust experimental outcomes and reproducibility. Furthermore, these cell lines can be customized to different research focuses, heightening their utility across various experimental paradigms.
For researchers, clinicians, and pharmaceutical companies focused on vision research or genetic disorders, CNGA1 Gene Knockout Cell Lines represent an invaluable resource. By providing insights into the pathogenic mechanisms underlying retinal diseases, these models can drive the development of innovative therapeutic strategies, fostering advancements in treatment options for affected individuals.
Our company is dedicated to providing high-quality, reliable biological products for researchers worldwide. With expertise in cell line development and gene editing, we stand behind the integrity and functionality of our CNGA1 Gene Knockout Cell Lines, ensuring they meet the demands of cutting-edge research.
Please note that all services are for research use only. Not intended for any clinical use.
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