Gene: KRT10
Official Full Name: keratin 10provided by HGNC
Gene Summary: This gene encodes a member of the type I (acidic) cytokeratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. Mutations in this gene are associated with epidermolytic hyperkeratosis. This gene is located within a cluster of keratin family members on chromosome 17q21. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36884 | KRT10 Knockout cell line (HeLa) | Human | KRT10 | 1:3~1:6 | Negative | Online Inquiry |
KO36885 | KRT10 Knockout cell line (HCT 116) | Human | KRT10 | 1:2~1:4 | Negative | Online Inquiry |
KO36886 | KRT10 Knockout cell line (HEK293) | Human | KRT10 | 1:3~1:6 | Negative | Online Inquiry |
KO36887 | KRT10 Knockout cell line (A549) | Human | KRT10 | 1:3~1:4 | Negative | Online Inquiry |
KRT10 Gene Knockout Cell Lines are genetically engineered cell lines in which the KRT10 gene, responsible for encoding keratin 10, is disrupted or inserted with a selectable marker. This innovative product allows researchers to study the functional roles of keratin proteins, particularly their influence on epithelial cell integrity, differentiation, and responses to mechanical stress. By employing CRISPR-Cas9 technology or similar genome editing techniques, these cell lines provide a robust and reproducible model system for examining keratin-related biological processes and pathologies.
The primary mechanism of action involves the complete deletion or modification of the KRT10 gene, leading to altered keratin expression and cellular behavior. This allows for the dissection of keratin's role in skin and epithelial health, offering insights into conditions such as epidermolytic ichthyosis, psoriasis, and other keratin-related disorders. The precise knockout enables researchers to observe changes in cytoskeletal architecture, signaling pathways, and cell-to-cell interactions under various experimental conditions.
From a scientific standpoint, KRT10 Gene Knockout Cell Lines are invaluable for both basic and applied research. They serve as a powerful tool for understanding keratin function, drug screening, and validation of therapeutic targets. Additionally, their application extends to regenerative medicine and tissue engineering for developing bioengineered skin substitutes or understanding wound healing mechanisms.
One significant competitive advantage of our KRT10 Gene Knockout Cell Lines is their high specificity and efficiency, which minimizes off-target effects often associated with traditional knockout methods. Furthermore, comprehensive validation and characterization of these cell lines ensure that researchers receive optimized models that enhance reproducibility and reliability in their experiments compared to alternative cell lines.
For researchers and clinicians seeking a deeper understanding of epithelial biology, developing new therapeutics, or exploring keratinopathies, our KRT10 Gene Knockout Cell Lines are a critical asset. They represent an intersection of innovation, precision, and scientific exploration. Our company, a leader in the development of genetic tools for cell biology, prioritizes quality and reliability by providing meticulously crafted products tailored to the evolving needs of the research community.
Please note that all services are for research use only. Not intended for any clinical use.
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