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NEFL Knockout Cell Lines

Gene: NEFL

Official Full Name: neurofilament light chainprovided by HGNC

Gene Summary: Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the light chain neurofilament protein. Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E), disorders of the peripheral nervous system that are characterized by distinct neuropathies. A pseudogene has been identified on chromosome Y. [provided by RefSeq, Oct 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00883 NEFL Knockout cell line(HCT 116) Human NEFL 1:2~1:4 Negative Online Inquiry
KO15778 NEFL Knockout cell line (HEK293) Human NEFL 1:3~1:6 Negative Online Inquiry
KO15779 NEFL Knockout cell line (A549) Human NEFL 1:3~1:4 Negative Online Inquiry

Background

NEFL Gene Knockout Cell Lines represent a cutting-edge tool in molecular biology used to study the neurofilament light chain (NEFL) gene, which plays a critical role in the structural integrity and function of neurons. These cell lines are genetically engineered to lack the NEFL gene, providing researchers with a unique model to investigate the implications of NEFL deficiency in neuronal health and disease. By observing cellular behavior in these knockout contexts, scientists can uncover the mechanisms underlying neurodegenerative disorders and other neurological conditions.

The primary function of the NEFL Gene Knockout Cell Lines lies in their ability to facilitate the examination of pathways impacted by the absence of the NEFL gene. Researchers can analyze changes in neurofilament assembly, axonal transport, and neuronal signaling, all of which are crucial for understanding neurobiology. The cell lines provide a controlled environment that mimics pathological states, allowing for the interrogation of cellular responses and the evaluation of therapeutic interventions aimed at neuroprotection and repair.

Scientifically, these knockout cell lines are invaluable for translational research and drug development, as they enable the identification and validation of targets for potential therapies aimed at conditions such as amyotrophic lateral sclerosis (ALS) and other motor neuron diseases. Additionally, they serve as a platform for screening pharmacological agents, assessing neurotoxic effects, and elucidating gene function, all of which contribute significantly to the advancement of neuroscience.

Compared to traditional cell lines or models, NEFL Gene Knockout Cell Lines offer distinct advantages including enhanced specificity in studying NEFL-related processes and an ability to produce reproducible results. Unlike other models that may exhibit variable gene expression levels, these knockout lines provide a uniform context that streamlines experimental design and analysis.

For researchers, clinicians, and pharmaceutical companies alike, NEFL Gene Knockout Cell Lines are an essential resource that fosters innovation in neurobiological research. Their unique capabilities allow for deeper insights into neuronal function and disease, ultimately guiding the development of novel therapeutic strategies.

Our company, with its extensive expertise in providing high-quality genetic tools, is committed to supporting scientific discovery through innovative product offerings like the NEFL Gene Knockout Cell Lines. We prioritize rigorous validation and user support, enabling our partners to achieve their research goals efficiently and effectively.

Please note that all services are for research use only. Not intended for any clinical use.

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