Gene: ZNF81
Official Full Name: zinc finger protein 81provided by HGNC
Gene Summary: This gene encodes a protein that likely functions as a transcription factor. The protein contains an N-terminal KRAB domain and several C2H2-type zinc finger motifs. Mutations in this gene cause an X-linked form of intellectual disability (MRX45). Microduplication of a region of chromosome X including this gene has also been associated with other forms of intellectual disability. [provided by RefSeq, Jul 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO34652 | ZNF81 Knockout cell line (HeLa) | Human | ZNF81 | 1:3~1:6 | Negative | Online Inquiry |
KO34653 | ZNF81 Knockout cell line (HCT 116) | Human | ZNF81 | 1:2~1:4 | Negative | Online Inquiry |
KO34654 | ZNF81 Knockout cell line (HEK293) | Human | ZNF81 | 1:3~1:6 | Negative | Online Inquiry |
KO34655 | ZNF81 Knockout cell line (A549) | Human | ZNF81 | 1:3~1:4 | Negative | Online Inquiry |
ZNF81 Gene Knockout Cell Lines are advanced model systems designed to facilitate the study of the ZNF81 gene, a crucial regulator implicated in various biological processes including transcriptional control, cell differentiation, and apoptosis. These cell lines are engineered using CRISPR/Cas9 technology, which allows for precise targeting and disruption of the ZNF81 gene, thereby enabling researchers to investigate its functions and the molecular pathways it influences.
The primary mechanism of these knockout cell lines involves the introduction of double-strand breaks in the ZNF81 gene sequence, which are then repaired inaccurately by the cellular repair machinery, resulting in frameshift mutations that inhibit functional protein production. This innovative approach provides a powerful tool for elucidating the gene's role in health and disease contexts and allows for the examination of phenotypic changes in gene expression, signaling pathways, and cellular behaviors.
The scientific importance of ZNF81 Gene Knockout Cell Lines extends to its applications in both fundamental research and translational studies. Researchers can use these models to explore ZNF81’s involvement in certain cancers, neurodegenerative diseases, and metabolic disorders. The ability to dissect the specific functions of ZNF81 enhances our understanding of its contributions to pathophysiology and may lead to the identification of novel therapeutic targets.
Compared to conventional methods of gene silencing such as siRNA or antisense oligonucleotides, our ZNF81 Gene Knockout Cell Lines offer several advantages. The CRISPR-generated knockout provides a stable genetic alteration that eliminates the gene’s expression entirely, rather than only reducing it. This complete ablation allows for a more rigorous analysis of gene function and the resultant phenotypes.
For researchers and clinicians, the value of ZNF81 Gene Knockout Cell Lines lies in their potential to drive innovations in genetic research and therapy development. These models not only facilitate the exploration of complex genetic interactions but also empower the design of next-generation therapies.
As a leader in genetic engineering solutions, our company harnesses cutting-edge technology and deep scientific expertise to offer ZNF81 Gene Knockout Cell Lines that meet the highest standards for accuracy and reliability, supporting your research endeavors with quality you can trust.
Please note that all services are for research use only. Not intended for any clinical use.
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