Home / CEP19 Knockout Cell Lines

CEP19 Knockout Cell Lines

Gene: CEP19

Official Full Name: centrosomal protein 19provided by HGNC

Gene Summary: The protein encoded by this gene localizes to centrosomes and primary cilia and co-localizes with a marker for the mother centriole. This gene resides in a region of human chromosome 3 that is linked to morbid obesity. A homozygous knockout of the orthologous gene in mouse resulted in mice with morbid obesity, hyperphagy, glucose intolerance, and insulin resistance. Mutations in this gene cause morbid obesity and spermatogenic failure (MOSPGF). This gene has a pseudogene on human chromosome 2. [provided by RefSeq, Apr 2014]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO24363 CEP19 Knockout cell line (HeLa) Human CEP19 1:3~1:6 Negative Online Inquiry
KO24364 CEP19 Knockout cell line (HCT 116) Human CEP19 1:2~1:4 Negative Online Inquiry
KO24365 CEP19 Knockout cell line (HEK293) Human CEP19 1:3~1:6 Negative Online Inquiry
KO24366 CEP19 Knockout cell line (A549) Human CEP19 1:3~1:4 Negative Online Inquiry

Background

CEP19 Gene Knockout Cell Lines are specialized cellular models that have been genetically engineered to lack the CEP19 gene, which encodes a protein implicated in the formation and function of cilia and centrosomes. This innovative tool enables researchers to study the biological consequences of CEP19 deficiency and its implications in various cellular processes, particularly in cell division, signaling pathways, and ciliary function.

Mechanistically, the CEP19 gene knockout alters the microtubule dynamics within the cells, leading to dysfunctional ciliogenesis and aberrant centro-some architecture. By utilizing these knockout cell lines, scientists can effectively investigate the roles that this gene and its associated pathways play in disease processes such as cancer, ciliopathies, and neurodegenerative disorders. The unique gene editing techniques, such as CRISPR-Cas9, employed to produce these knockout models ensure precise modifications, allowing for reliable and reproducible experimental results.

The scientific importance of CEP19 Gene Knockout Cell Lines extends to both research and clinical applications. In research settings, they serve as invaluable tools for elucidating the molecular mechanisms behind ciliary dysfunction and its relationship with various human diseases. Clinically, insights gained from experiments using these models may guide the development of targeted therapies and diagnostic tools for conditions linked to ciliary impairment.

What sets our CEP19 Gene Knockout Cell Lines apart from alternative models is their high purity and consistent performance. Our products undergo rigorous quality control to ensure optimal viability and functionality, providing researchers with reliable experimental systems for studying complex biological questions. Additionally, the ease of integration into existing experimental frameworks enhances their accessibility for laboratories of varying scales.

By investing in our CEP19 Gene Knockout Cell Lines, researchers and clinicians gain an essential resource that supports cutting-edge investigations and translational research. Our commitment to scientific excellence, combined with extensive expertise in the development of genetic cell lines, positions us as leaders in the biosciences market, dedicated to empowering scientific discovery and innovation.

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

Get a free quote

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.

0

There is no product in your cart.