Gene: DNAH11
Official Full Name: dynein axonemal heavy chain 11provided by HGNC
Gene Summary: This gene encodes a ciliary outer dynein arm protein and is a member of the dynein heavy chain family. It is a microtubule-dependent motor ATPase and has been reported to be involved in the movement of respiratory cilia. Mutations in this gene have been implicated in causing Kartagener Syndrome (a combination of situs inversus totalis and Primary Ciliary Dyskinesia (PCD), also called Immotile Cilia Syndrome 1 (ICS1)) and male sterility. [provided by RefSeq, Mar 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO33945 | DNAH11 Knockout cell line (HCT 116) | Human | DNAH11 | 1:2~1:4 | Negative | Online Inquiry |
KO33946 | DNAH11 Knockout cell line (HEK293) | Human | DNAH11 | 1:3~1:6 | Negative | Online Inquiry |
DNAH11 Gene Knockout Cell Lines are precisely engineered cellular models designed to facilitate the investigation of the DNAH11 gene's functional role in cellular processes. This product specifically enables the targeted disruption of the DNAH11 gene, which encodes a component of the axonemal dynein complex, critical for ciliary motility. By utilizing CRISPR/Cas9 technology, these cell lines are generated to exhibit a definitive knockout of DNAH11, allowing researchers to observe the resultant phenotype and its implications in various biological contexts.
The primary function of DNAH11 Gene Knockout Cell Lines is to serve as a tool for elucidating the molecular and cellular mechanisms associated with ciliary dysfunction, particularly in the context of human diseases such as primary ciliary dyskinesia (PCD). These models provide insight into how genetic mutations can lead to impaired ciliary movement, which is essential for various physiological processes including respiratory function and fertility. The knockout lines enable not only phenotypic analysis but also the potential for high-throughput screening of therapeutic compounds that could ameliorate the consequences of impaired ciliary function.
One of the most significant advantages of utilizing DNAH11 Gene Knockout Cell Lines is the specificity and precision of the gene editing process, leading to more reliable and reproducible results compared to traditional knockdown approaches. This specificity reduces off-target effects, thereby increasing the validity of experimental outcomes. Furthermore, the availability of these cell lines accelerates research timelines and facilitates the investigation of both basic and applied research questions in cellular biology, genetics, and potential therapeutic strategies.
For researchers and clinicians, these knockout cell lines stand as invaluable resources in both academic and industrial settings. They offer a unique opportunity to explore the pathophysiology of diseases tied to ciliary defects, thereby informing the development of novel therapies and interventions.
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