Gene: KIRREL3
Official Full Name: kirre like nephrin family adhesion molecule 3provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the nephrin-like protein family. These proteins are expressed in fetal and adult brain, and also in podocytes of kidney glomeruli. The cytoplasmic domains of these proteins interact with the C-terminus of podocin, also expressed in the podocytes, cells involved in ensuring size- and charge-selective ultrafiltration. The protein encoded by this gene is a synaptic cell adhesion molecule with multiple extracellular immunoglobulin-like domains and a cytoplasmic PDZ domain-binding motif. Mutations in this gene are associated with several neurological and cognitive disorders. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO24770 | KIRREL3 Knockout cell line (HeLa) | Human | KIRREL3 | 1:3~1:6 | Negative | Online Inquiry |
KO24771 | KIRREL3 Knockout cell line (A549) | Human | KIRREL3 | 1:3~1:4 | Negative | Online Inquiry |
KIRREL3 Gene Knockout Cell Lines are genetically modified cell lines that have been engineered to express a complete knockout of the KIRREL3 gene, which encodes a member of the immunoglobulin superfamily, playing vital roles in synaptic development and neuronal connectivity. These cell lines provide researchers with a powerful tool for exploring the cellular pathways and molecular mechanisms associated with KIRREL3 functions, particularly in neurobiology and developmental biology.
The primary mechanism by which KIRREL3 knockout occurs involves the targeted disruption of the KIRREL3 gene through CRISPR-Cas9 technology. This precise gene-editing approach enables the introduction of insertions or deletions within the genomic DNA, leading to a loss-of-function phenotype that is critical for studying the gene's role in cellular processes and disease models. As a result, researchers can investigate the implications of KIRREL3 deficiency, particularly in relation to neurodevelopmental disorders and other pathologies linked to aberrant cellular signaling.
The scientific importance of KIRREL3 Gene Knockout Cell Lines lies in their capacity to advance our understanding of the genetic underpinnings of diseases. They provide a robust model for drug discovery, functional genomics, and personalized medicine applications. In clinical settings, these knockout models facilitate the investigation of potential therapeutic targets and biomarkers associated with neurodevelopmental conditions, enabling translational research efforts that could lead to novel treatments.
Compared to other gene editing or knockout models, KIRREL3 Gene Knockout Cell Lines offer distinct advantages such as validated genetic modifications, reproducible phenotypes, and ease of use for downstream assays. These cell lines save time and resources, allowing researchers to focus on analysis rather than the complex process of creating and validating knockout models.
Given the increasing relevance of genetic factors in health and disease, KIRREL3 Gene Knockout Cell Lines stand out as an invaluable resource for researchers and clinicians alike. These lines are not only pivotal for fundamental research but are also critical for developing innovative therapeutic strategies. With our extensive experience in gene editing technologies and commitment to supporting scientific advancement, our company is dedicated to providing high-quality biological products that empower researchers to make groundbreaking discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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