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NF2 Knockout Cell Lines

Gene: NF2

Official Full Name: NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressorprovided by HGNC

Gene Summary: This gene encodes a protein that is similar to some members of the ERM (ezrin, radixin, moesin) family of proteins that link cytoskeletal components with proteins in the cell membrane. The encoded protein is involved in regulation of contact-dependent inhibition of cell proliferation and functions in cell-cell adhesion and transmembrane signaling. The encoded protein has been shown to interact with cell-surface proteins, proteins involved in cytoskeletal dynamics, and proteins involved in regulating ion transport. Disruption of this protein's function has been implicated in tumorigenesis and metastasis. Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities. [provided by RefSeq, May 2022]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO08611 NF2 Knockout cell line (HeLa) Human NF2 1:3~1:6 Negative Online Inquiry
KO08612 NF2 Knockout cell line (HCT 116) Human NF2 1:2~1:4 Negative Online Inquiry
KO08613 NF2 Knockout cell line (HEK293) Human NF2 1:3~1:6 Negative Online Inquiry
KO08614 NF2 Knockout cell line (A549) Human NF2 1:3~1:4 Negative Online Inquiry

Background

NF2 Gene Knockout Cell Lines are meticulously engineered cell lines designed to facilitate the study of Neurofibromatosis type 2 (NF2), a genetic disorder characterized by the development of bilateral vestibular schwannomas and other tumors. By utilizing CRISPR/Cas9 technology, these cell lines have been specifically modified to knock out the NF2 gene, allowing researchers to elucidate the gene's function and its role in tumorigenesis. The resultant cell lines provide an invaluable model for examining the pathways and cellular mechanisms affected by NF2 loss, permitting targeted investigations into the biology of schwannomas and associated neoplasms.

The primary mechanisms of action involve the disruption of the merlin protein, which is encoded by the NF2 gene and plays a critical role in cell signaling, tumor suppression, and cellular adhesion. By studying the NF2 knockout phenotype, researchers can gain insights into cell proliferation, migration, and apoptosis, which are crucial for developing targeted therapies to treat NF2-related tumors.

From a scientific perspective, these cell lines are pivotal tools for advancing cancer research and therapeutic development. They hold significant potential for drug screening and discovering novel therapeutic targets, offering a platform to test the efficacy of anti-tumor compounds in an NF2-deficient context. Their application extends to understanding other cancers where NF2 mutations may play a role, bridging the gap between basic research and clinical innovations.

One central advantage of our NF2 Gene Knockout Cell Lines is their reliability and reproducibility, compared to traditional knockout models, which can often be time-consuming and less efficient. These cell lines have undergone rigorous validation to ensure the precision of the gene editing, thus providing researchers with a consistent and robust resource. Additionally, they are readily available, eliminating the lengthy process of generating new models.

For researchers and clinicians eager to explore the complexities of NF2-related tumors, these knockout cell lines represent an unparalleled opportunity to accelerate discovery and contribute meaningful advancements in cancer biology. By leveraging our expertise in gene editing technology and cellular biology, our company consistently delivers high-quality biological products that empower the scientific community to push boundaries and explore new frontiers in health and disease research.

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

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