Gene: ZNF57
Official Full Name: zinc finger protein 57provided 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 active in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO27388 | ZNF57 Knockout cell line (HeLa) | Human | ZNF57 | 1:3~1:6 | Negative | Online Inquiry |
KO27389 | ZNF57 Knockout cell line (HCT 116) | Human | ZNF57 | 1:2~1:4 | Negative | Online Inquiry |
KO27390 | ZNF57 Knockout cell line (HEK293) | Human | ZNF57 | 1:3~1:6 | Negative | Online Inquiry |
KO27391 | ZNF57 Knockout cell line (A549) | Human | ZNF57 | 1:3~1:4 | Negative | Online Inquiry |
ZNF57 Gene Knockout Cell Lines are genetically engineered cell lines designed to specifically disrupt the ZNF57 gene, a critical regulator of genomic imprinting, which facilitates the expression of genes in a parent-of-origin manner. These cell lines are indispensable research tools that allow scientists to investigate the functional role of ZNF57 within various biological processes, including cellular differentiation, growth regulation, and epigenetic modifications.
The mechanism underlying the functionality of ZNF57 knockout cell lines involves the use of CRISPR-Cas9 technology or similar genome-editing approaches to introduce precise mutations that inactivate the ZNF57 gene. By assessing the phenotypic changes and molecular alterations in these cell lines, researchers can elucidate the pathways influenced by ZNF57 and explore its implications in disorders linked to genomic imprinting, such as Prader-Willi syndrome and Angelman syndrome. Thus, these cell lines not only advance our understanding of fundamental genetic processes but also offer potential insights for therapeutic interventions.
Scientific importance is underscored by the role of ZNF57 in epigenetic regulation, with implications that stretch from basic biology to clinical applications. The ZNF57 knockout cell lines are particularly valuable for drug discovery, genetic studies, and the development of gene therapies aimed at correcting imprinting disorders.
Compared to conventional models, the ZNF57 knockout cell lines exhibit distinct advantages, including enhanced specificity and reduced off-target effects. The controlled genetic environment provided by these cell lines allows for robust and reproducible results, making them a superior choice for researchers focused on precision genetics.
For researchers and clinicians who aim to explore the intricacies of genomic regulation and imprinting disorders, ZNF57 Gene Knockout Cell Lines represent a significant step forward. They not only facilitate groundbreaking research but also support the development of innovative therapeutic strategies.
As a leading provider of high-quality genetic tools, our expertise in cell line engineering and commitment to scientific excellence ensure that researchers receive reliable products that meet rigorous standards, advancing the frontier of genetic and biomedical research.
Please note that all services are for research use only. Not intended for any clinical use.
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