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TMEM216 Knockout Cell Lines

Gene: TMEM216

Official Full Name: transmembrane protein 216provided by HGNC

Gene Summary: This locus encodes a transmembrane domain-containing protein. Mutations at this locus have been associated with Meckel-Gruber Syndrome Type 2, and Joubert Syndrome 2, also known as Cerebello-oculorenal Syndrome 2. [provided by RefSeq, Aug 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO22762 TMEM216 Knockout cell line (HeLa) Human TMEM216 1:3~1:6 Negative Online Inquiry
KO22763 TMEM216 Knockout cell line (HCT 116) Human TMEM216 1:2~1:4 Negative Online Inquiry
KO22764 TMEM216 Knockout cell line (HEK293) Human TMEM216 1:3~1:6 Negative Online Inquiry
KO22765 TMEM216 Knockout cell line (A549) Human TMEM216 1:3~1:4 Negative Online Inquiry

Background

TMEM216 Gene Knockout Cell Lines are genetically engineered cell lines characterized by the complete ablation of the TMEM216 gene. The TMEM216 gene is associated with the transport of proteins within cells and has implications in various cellular functions, including ciliary assembly and cell signaling pathways. By utilizing these knockout cell lines, researchers can effectively study the specific roles of TMEM216 in cellular processes, model diseases related to ciliary dysfunction, and investigate the impact of gene loss on cellular behavior.

The primary function of TMEM216 Gene Knockout Cell Lines lies in their ability to mimic the pathological states seen in certain genetic disorders, particularly those involving ciliary dysfunction, such as ciliopathies. The knockout mechanism is achieved through CRISPR-Cas9 technology, ensuring precise editing and elimination of the gene of interest. This leads to observable phenotypic changes that researchers can measure, such as altered cell motility, proliferation, and differentiation, providing insights into the underlying mechanisms of disease.

In scientific research and clinical settings, these cell lines serve as invaluable tools for understanding the biological pathways implicated in multiple disorders. The TMEM216 knockout phenotype allows for high-throughput drug screening, potential gene therapy studies, or the development of novel therapeutic strategies. Moreover, they are instrumental in advancing our comprehension of ciliary function and its disruption in various diseases.

Compared to conventional methods of studying gene function, such as RNA interference or wild-type cell lines, TMEM216 Gene Knockout Cell Lines offer unparalleled specificity. A complete gene knockout permits researchers to definitively elucidate the gene's role within biological contexts, eliminating off-target effects often associated with alternative methods.

The value of these cell lines is amplified by the adaptability of their applications, which extend across diverse fields including neurobiology, developmental biology, and disease modeling. By providing comprehensive insights into genetic contributions to cellular function and pathology, TMEM216 Gene Knockout Cell Lines are essential assets for researchers and clinicians alike.

At our company, we specialize in delivering high-quality, rigorously validated biological products, including these innovative knockout cell lines, focusing on empowering the scientific community to push the boundaries of genetic research and therapeutic development.

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

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