Gene: MSANTD5
Official Full Name: Myb/SANT DNA binding domain containing 5provided by HGNC
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO16013 | MSANTD5 Knockout cell line (HeLa) | Human | MSANTD5 | 1:3~1:6 | Negative | Online Inquiry |
KO16014 | MSANTD5 Knockout cell line (HCT 116) | Human | MSANTD5 | 1:2~1:4 | Negative | Online Inquiry |
KO16015 | MSANTD5 Knockout cell line (A549) | Human | MSANTD5 | 1:3~1:4 | Negative | Online Inquiry |
MSANTD5 Gene Knockout Cell Lines are a specialized type of cellular model engineered to lack the MSANTD5 gene, providing crucial insights into its biological functions and implications in various cellular processes. These knockout cell lines are created using advanced genetic engineering techniques that result in the targeted disruption of the MSANTD5 gene, a regulatory element associated with critical pathways in cell differentiation and proliferation. By eliminating this gene, researchers can observe the resulting phenotypic changes and elucidate the role of MSANTD5 in health and disease.
The key functions of MSANTD5 Gene Knockout Cell Lines involve providing a platform for studying the gene's involvement in cellular signaling, metabolic pathways, and disease models, particularly in cancer biology and regenerative medicine. The precise mechanism underlying the alteration of cellular behavior upon MSANTD5 knockout can ultimately lead to the identification of novel therapeutic targets, enhancing the understanding of various pathologies.
Scientifically, these cell lines are invaluable in research contexts, offering researchers and clinicians the ability to explore the action of MSANTD5 in cellular models relevant to both basic and applied sciences. They enable high-throughput screening of pharmacological agents and the assessment of gene-drug interactions, facilitating the development of new therapies.
Compared to alternative models, MSANTD5 Gene Knockout Cell Lines provide a specific approach to understanding gene function that traditional models—like wild-type or overexpressing lines—cannot yield. Their application in pharmacogenomics and precision medicine positions them as a pivotal tool for elucidating patient-specific therapeutic responses.
This product is exceptionally valuable to researchers and clinicians who are keen to unravel the complexities of gene function in health and disease, thereby contributing to advancements in molecular biology and translational research. Our company prides itself on its expertise in the development of innovative biological tools, enabling breakthroughs in life sciences through cutting-edge technologies and exceptional product quality.
Please note that all services are for research use only. Not intended for any clinical use.
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