Gene: ZNF408
Official Full Name: zinc finger protein 408provided by HGNC
Gene Summary: The protein encoded by this gene contains ten tandem zinc fingers and an N-terminal SET domain, so it is likely a DNA binding protein that interacts with other proteins. In adults, the encoded protein is expressed most highly in retina. Consequently, defects in this gene have been associated with familial exudative vitreoretinopathy (FEVR) and retinitis pigmentosa (RP). [provided by RefSeq, Dec 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO12259 | ZNF408 Knockout cell line (HeLa) | Human | ZNF408 | 1:3~1:6 | Negative | Online Inquiry |
KO12260 | ZNF408 Knockout cell line (HCT 116) | Human | ZNF408 | 1:2~1:4 | Negative | Online Inquiry |
KO12261 | ZNF408 Knockout cell line (HEK293) | Human | ZNF408 | 1:3~1:6 | Negative | Online Inquiry |
KO12262 | ZNF408 Knockout cell line (A549) | Human | ZNF408 | 1:3~1:4 | Negative | Online Inquiry |
ZNF408 Gene Knockout Cell Lines are specifically engineered cellular models designed to lack the ZNF408 gene, a key regulator in various biological processes, particularly those involved in genomic stability and protein-DNA interactions. By utilizing CRISPR-Cas9 technology, these cell lines demonstrate a precise and efficient method for the disruption of the ZNF408 gene, allowing researchers to investigate the gene's functions and its impact on cellular behavior.
The primary mechanism of these cell lines revolves around the gene-editing capabilities of the CRISPR-Cas9 system, which utilizes a guide RNA to target the ZNF408 locus, subsequently creating double-strand breaks repaired by erroneous non-homologous end joining. This results in a knockout of the gene, facilitating the study of phenotypic changes in various cellular contexts such as cell proliferation, apoptosis, and stress responses. This type of model is invaluable in dissecting the role of ZNF408 in oncogenic pathways and potential tumorigenesis.
The scientific importance of ZNF408 gene knockout cell lines extends to various research domains, including cancer biology, regenerative medicine, and stem cell research. By providing insights into gene functions and interactions, these models can support drug development initiatives and therapeutics targeting disease-modifying pathways. In clinical settings, these cell lines serve as crucial tools for validating the efficacy of novel compounds aimed at modulating ZNF408-related pathways.
What sets ZNF408 Gene Knockout Cell Lines apart from alternative models is their designer precision and the versatility they offer. Unlike traditional knockdown methods, which may yield partial reductions in gene activity, these knockout lines enable a complete abrogation of gene function, yielding clearer interpretations of functional analyses. Furthermore, their reproducibility and consistency across experiments enhance their reliability as experimental tools.
In summary, ZNF408 Gene Knockout Cell Lines are an essential asset for researchers and clinicians striving to advance our understanding of genetic regulation and cellular dynamics in disease contexts. With a firm commitment to innovation, our company specializes in the development of high-fidelity biological products designed to empower scientific discovery, making a mark in the realm of genome editing technology.
Please note that all services are for research use only. Not intended for any clinical use.
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