Gene: INPP5E
Official Full Name: inositol polyphosphate-5-phosphatase Eprovided by HGNC
Gene Summary: The protein encoded by this gene is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase. InsP3 5-phosphatases hydrolyze Ins(1,4,5)P3, which mobilizes intracellular calcium and acts as a second messenger mediating cell responses to various stimulation. Studies of the mouse counterpart suggest that this protein may hydrolyze phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,5-bisphosphate on the cytoplasmic Golgi membrane and thereby regulate Golgi-vesicular trafficking. Mutations in this gene cause Joubert syndrome; a clinically and genetically heterogenous group of disorders characterized by midbrain-hindbrain malformation and various associated ciliopathies that include retinal dystrophy, nephronophthisis, liver fibrosis and polydactyly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO07911 | INPP5E Knockout cell line (HeLa) | Human | INPP5E | 1:3~1:6 | Negative | Online Inquiry |
KO07912 | INPP5E Knockout cell line (HCT 116) | Human | INPP5E | 1:2~1:4 | Negative | Online Inquiry |
KO07913 | INPP5E Knockout cell line (HEK293) | Human | INPP5E | 1:3~1:6 | Negative | Online Inquiry |
KO07914 | INPP5E Knockout cell line (A549) | Human | INPP5E | 1:3~1:4 | Negative | Online Inquiry |
INPP5E Gene Knockout Cell Lines are specifically engineered cellular models that functionally inactivate the inositol polyphosphate-5-phosphatase E (INPP5E) gene. This gene plays a pivotal role in phosphoinositide metabolism, which is critical for various cellular signaling pathways. By utilizing CRISPR/Cas9 technology, these cell lines allow researchers to achieve precise gene editing, resulting in the deletion or modification of the INPP5E gene. The resulting knockout cell lines exhibit altered signaling cascades that are instrumental in the study of neurodevelopmental disorders, ciliary function, and various cancer pathways.
The core functionality of these knockout cell lines lies in their ability to provide a simplified model for studying the downstream effects of INPP5E deficiency. Researchers can investigate alterations in cellular processes like membrane trafficking, cell proliferation, and apoptosis, subsequently allowing for the identification of potential therapeutic targets. These applications are particularly significant in both fundamental research and drug discovery, where INPP5E has been implicated in conditions such as Joubert syndrome and other ciliopathies.
What sets our INPP5E Gene Knockout Cell Lines apart from other similar products is their high efficiency in gene editing and the robust characterization that accompanies each cell line. Our lines are extensively validated, ensuring reproducibility in experiments, which is a critical factor for obtaining reliable data. Moreover, they come with a comprehensive data package that delineates the expected cellular behavior post-knockout, facilitating a smoother integration into ongoing research projects.
Researchers and clinicians will find these cell lines invaluable because they not only expedite the process of studying INPP5E-related mechanisms but also help bridge the gap between basic research and potential clinical applications. They stand as powerful tools in the quest to unravel the complexities of cellular signaling and disease pathogenesis.
Our company has a proven track record of producing high-quality biological products, backed by years of expertise in gene editing technologies. We are committed to providing cutting-edge tools that empower researchers and clinicians to advance their work in understanding and treating diseases at the molecular level.
Please note that all services are for research use only. Not intended for any clinical use.
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