Gene: NEURL1
Official Full Name: neuralized E3 ubiquitin protein ligase 1provided by HGNC
Gene Summary: Predicted to enable translation factor activity, non-nucleic acid binding and ubiquitin protein ligase activity. Involved in negative regulation of Notch signaling pathway; negative regulation of cell population proliferation; and positive regulation of apoptotic process. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO33526 | NEURL1 Knockout cell line (HeLa) | Human | NEURL1 | 1:3~1:6 | Negative | Online Inquiry |
KO33527 | NEURL1 Knockout cell line (HCT 116) | Human | NEURL1 | 1:2~1:4 | Negative | Online Inquiry |
KO33528 | NEURL1 Knockout cell line (HEK293) | Human | NEURL1 | 1:3~1:6 | Negative | Online Inquiry |
NEURL1 Gene Knockout Cell Lines are genetically modified cell lines in which the NEURL1 gene has been inactivated or "knocked out." This specific gene is implicated in various cellular processes, including neuronal differentiation and synaptic function. By employing advanced CRISPR/Cas9 gene-editing technology, the NEURL1 gene knockout provides researchers with a robust tool to investigate the biological roles and signaling pathways mediated by NEURL1 in both normal physiology and disease states.
The primary function of NEURL1 gene knockout cell lines is to facilitate detailed studies on the cellular mechanisms underlying neurological disorders, particularly those related to synaptic dysfunction and neurodevelopmental abnormalities. By inhibiting NEURL1 expression, scientists can observe phenotypic changes, assess effects on protein interactions, and explore the cell’s response to various stimuli. This knowledge is crucial for unraveling the complexity of neurobiology and developing targeted therapeutic strategies.
The scientific importance of NEURL1 gene knockout cell lines extends to numerous research applications, including drug discovery, toxicology studies, and the examination of genetic interactions. By providing a unique model for investigating the implications of NEURL1 deficiency, these cell lines enable researchers to identify potential biomarkers for disease and to evaluate new treatment modalities in a controlled environment.
What sets our NEURL1 gene knockout cell lines apart from alternative products is the precision of our gene-editing technique, which ensures high specificity and minimal off-target effects. Moreover, our cell lines are fully validated and come with detailed characterization data, enhancing their reliability for experimental applications. This level of rigor delivers exceptional confidence for researchers aiming to publish their findings or contribute to clinical studies.
For researchers and clinicians focusing on neurobiology, understanding NEURL1's role can unveil new pathways for intervention in complex neurological disorders. Our NEURL1 gene knockout cell lines are not merely tools; they are critical enablers of scientific discovery, with the potential to contribute significantly to the advancement of therapeutic approaches.
Our company is dedicated to providing high-quality biological products backed by cutting-edge technology and rigorous scientific validation. With a commitment to innovation and excellence, we aim to support the research community in making meaningful advancements in healthcare and therapeutic development.
Please note that all services are for research use only. Not intended for any clinical use.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
There is no product in your cart. |
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.