Gene: ZMYND12
Official Full Name: zinc finger MYND-type containing 12provided by HGNC
Gene Summary: Predicted to enable metal ion binding activity. Involved in sperm axoneme assembly. Located in sperm flagellum. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO25086 | ZMYND12 Knockout cell line (HCT 116) | Human | ZMYND12 | 1:2~1:4 | Negative | Online Inquiry |
ZMYND12 Gene Knockout Cell Lines are genetically engineered cell lines that have been engineered to lack the ZMYND12 gene, a crucial regulator involved in various cellular processes including transcriptional regulation and chromatin remodeling. By utilizing CRISPR/Cas9 gene-editing technology, these knockout cell lines provide researchers with a powerful tool to investigate the role of ZMYND12 in cellular functions, pathogenesis, and the development of diseases.
The fundamental mechanism of ZMYND12 involves its interaction with specific histone modifications and other proteins associated with gene expression. By knocking out this gene, researchers can explore alterations in gene expression patterns, chromatin accessibility, and downstream signaling cascades, leading to a deeper understanding of cellular responses under various conditions. The ZMYND12 knockout model serves as an essential platform to study cancer biology, as perturbations in its function have been linked to tumorigenesis and the response to therapeutic agents.
Scientifically, the ZMYND12 Gene Knockout Cell Lines are invaluable in both research and clinical settings. They enable the exploration of the knockout effects on cell proliferation, differentiation, and metastasis in cancer models, thus opening avenues for novel therapeutic strategies. Additionally, these cell lines can be employed in drug discovery processes to identify potential pharmacological targets influenced by the absence of ZMYND12.
Distinct advantages include their reproducibility and ease of use relative to traditional methods of gene manipulation, such as shRNA or siRNA knockdown, which may result in incomplete gene suppression. Furthermore, researchers can confidently rely on well-characterized backgrounds to minimize variability in experimental setups.
This product holds significant value for researchers and clinicians alike, providing clarity on the biological functions of ZMYND12, which may ultimately contribute to advances in personalized medicine and therapeutic interventions. Our company is dedicated to delivering high-quality biological products, backed by years of expertise in gene editing and cellular biology, ensuring that our clients have access to the most reliable tools for their research initiatives.
Please note that all services are for research use only. Not intended for any clinical use.
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