Gene: NPHP3
Official Full Name: nephrocystin 3provided by HGNC
Gene Summary: This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene. [provided by RefSeq, Feb 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO27906 | NPHP3 Knockout cell line (HeLa) | Human | NPHP3 | 1:3~1:6 | Negative | Online Inquiry |
KO27907 | NPHP3 Knockout cell line (HCT 116) | Human | NPHP3 | 1:2~1:4 | Negative | Online Inquiry |
KO27908 | NPHP3 Knockout cell line (HEK293) | Human | NPHP3 | 1:3~1:6 | Negative | Online Inquiry |
KO27909 | NPHP3 Knockout cell line (A549) | Human | NPHP3 | 1:3~1:4 | Negative | Online Inquiry |
NPHP3 Gene Knockout Cell Lines represent a powerful tool in molecular biology, designed for the in-depth study of the nephronophthisis 3 (NPHP3) gene. These cell lines are specifically engineered to facilitate the investigation of NPHP3's role in kidney function and disease, particularly in the context of renal ciliopathies. Through the targeted deletion of the NPHP3 gene, these knockout cell lines provide researchers with a unique platform to analyze the resultant phenotypic changes at both cellular and molecular levels.
The primary function of NPHP3 is believed to be integral in the maintenance of primary cilia, which are essential for proper kidney development and function. By utilizing these knockout cell lines, researchers can elucidate the mechanisms by which NPHP3 contributes to ciliary assembly and signaling pathways that regulate cellular homeostasis. This can have significant implications in understanding diseases associated with cilia dysfunction, such as cystic kidney disease, thereby advancing potential therapeutic strategies.
In terms of scientific importance, NPHP3 Gene Knockout Cell Lines are invaluable in both research and clinical settings. They serve as a cornerstone for functional studies that aim to uncover the biological pathways affected by NPHP3 knockout, enabling the identification of novel biomarkers or drug targets related to renal diseases. Furthermore, these cell lines can be employed in screening assays for potential therapeutic compounds that can restore the function of disrupted pathways, accelerating advancements in nephrology.
One specific advantage of our NPHP3 Gene Knockout Cell Lines is their high degree of specificity and reliability, ensuring reproducible results that are often challenged by other models, such as traditional wild-type cell lines or animal models. The knockout efficiency is verified through robust genotyping methods, providing confidence in experimental outcomes.
Ultimately, the NPHP3 Gene Knockout Cell Lines are an essential tool for researchers and clinicians committed to advancing the understanding of kidney disease mechanisms. Their detailed characterization and experimental fidelity position them as superior alternatives to existing models, unlocking vital insights into nephronophthisis and related disorders.
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Please note that all services are for research use only. Not intended for any clinical use.
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