Gene: ZNF566
Official Full Name: zinc finger protein 566provided by HGNC
Gene Summary: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO24468 | ZNF566 Knockout cell line (HeLa) | Human | ZNF566 | 1:3~1:6 | Negative | Online Inquiry |
KO24469 | ZNF566 Knockout cell line (HCT 116) | Human | ZNF566 | 1:2~1:4 | Negative | Online Inquiry |
KO24470 | ZNF566 Knockout cell line (HEK293) | Human | ZNF566 | 1:3~1:6 | Negative | Online Inquiry |
KO24471 | ZNF566 Knockout cell line (A549) | Human | ZNF566 | 1:3~1:4 | Negative | Online Inquiry |
ZNF566 Gene Knockout Cell Lines represent a revolutionary tool in the field of genetic research, specifically designed to facilitate the study of the ZNF566 gene and its associated biological pathways. These cell lines are engineered through the precise application of CRISPR-Cas9 technology, which enables targeted disruption of the ZNF566 gene, resulting in the elimination of its expression. The knockout functionality allows researchers to investigate the phenotypic consequences of ZNF566 loss, contributing to our understanding of its role in cellular processes and disease mechanisms.
The key mechanism behind ZNF566 knockout cell lines involves the introduction of double-strand breaks in the genomic DNA at specific sites within the ZNF566 locus. Following the introduction of these breaks, the cell's inherent repair mechanisms often result in insertions or deletions that lead to a frame shift, effectively generating a non-functional allele. This alteration enables researchers to explore the functional implications of gene silencing, as well as the potential compensatory pathways that may come into play.
The scientific importance of ZNF566 Gene Knockout Cell Lines extends broadly into research domains such as oncology, developmental biology, and neurobiology. By elucidating the role of ZNF566 in pathological states, these models are invaluable for identifying novel therapeutic targets and understanding disease mechanisms, thereby accelerating the translation of research findings into clinical applications.
What sets our ZNF566 Gene Knockout Cell Lines apart from alternatives is the precision of the knockout, the assurance of extensive validation, and the support of comprehensive usage protocols. These advantages not only streamline research processes but also enhance reproducibility and reliability, crucial aspects of scientific inquiry.
For researchers and clinicians alike, the ZNF566 Gene Knockout Cell Lines offer profound value as they provide a robust platform for advancing knowledge and developing innovative treatments. Our commitment to delivering high-quality biological products is backed by years of expertise in genetic engineering and a dedication to supporting the scientific community. By investing in our ZNF566 Gene Knockout Cell Lines, users gain access to state-of-the-art resources that empower their research endeavors and catalyze transformative discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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