Gene: RPGRIP1L
Official Full Name: RPGRIP1 likeprovided by HGNC
Gene Summary: The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO29464 | RPGRIP1L Knockout cell line (HeLa) | Human | RPGRIP1L | 1:3~1:6 | Negative | Online Inquiry |
KO29465 | RPGRIP1L Knockout cell line (HCT 116) | Human | RPGRIP1L | 1:2~1:4 | Negative | Online Inquiry |
KO29466 | RPGRIP1L Knockout cell line (HEK293) | Human | RPGRIP1L | 1:3~1:6 | Negative | Online Inquiry |
KO29467 | RPGRIP1L Knockout cell line (A549) | Human | RPGRIP1L | 1:3~1:4 | Negative | Online Inquiry |
RPGRIP1L Gene Knockout Cell Lines represent a pivotal advancement in cellular biology, designed specifically to facilitate the study of the RPGRIP1L gene's functions and its implications in human disease, particularly in various ciliopathies. These cell lines are engineered to lack the RPGRIP1L gene, providing a crucial tool for researchers to analyze the biological pathways and mechanisms regulated by this gene, which plays a vital role in the formation and function of cilia.
The key functions of RPGRIP1L include its involvement in the assembly and maintenance of primary cilia, which are essential for various signaling pathways, including the Hedgehog signaling pathway. By utilizing these knockout cell lines, scientists can investigate the perturbations in cellular signaling that occur in the absence of RPGRIP1L, leading to a deeper understanding of its role in both developmental biology and pathology.
Scientific importance is underscored by the growing recognition of ciliopathies and their diverse clinical manifestations, such as renal diseases, retinal degeneration, and developmental disorders. The RPGRIP1L Gene Knockout Cell Lines enable researchers to model these conditions accurately, thus paving the way for potential therapeutic interventions and biomarker discovery.
Uniquely, our cell lines offer a reliable and reproducible model, equipped with characterized phenotypic alterations, unlike other models that may be subject to variability. This specificity can lead to more consistent and reliable results, enhancing the translational potential of research findings.
For researchers and clinicians focused on genetic, developmental, and cell biology, RPGRIP1L Gene Knockout Cell Lines present an invaluable resource. They facilitate innovative experimentation, help delineate complex biological interactions, and drive forward the understanding of a critical gene's role in health and disease.
At our company, we pride ourselves on our commitment to advancing biomedical research through the development of high-quality, genetically optimized biological products, ensuring that our offerings remain at the forefront of scientific exploration.
Please note that all services are for research use only. Not intended for any clinical use.
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