Gene: KRT5
Official Full Name: keratin 5provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the basal layer of the epidermis with family member KRT14. Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05456 | KRT5 Knockout cell line (HeLa) | Human | KRT5 | 1:3~1:6 | Negative | Online Inquiry |
KO05457 | KRT5 Knockout cell line (HCT 116) | Human | KRT5 | 1:2~1:4 | Negative | Online Inquiry |
KO05458 | KRT5 Knockout cell line (A549) | Human | KRT5 | 1:3~1:4 | Negative | Online Inquiry |
KRT5 Gene Knockout Cell Lines are genetically engineered cell lines in which the keratin 5 (KRT5) gene has been selectively disrupted. The KRT5 protein plays a crucial role in the structural integrity and function of epithelial tissues, particularly in the basal layer of stratified epithelia, including the epidermis. By generating knockout models, researchers can precisely investigate the implications of KRT5 loss on cellular behavior and differentiation, providing insight into the molecular underpinnings of skin disorders and various carcinomas.
These cell lines function by utilizing CRISPR/Cas9 gene editing technology, which allows for specific and efficient induction of double-stranded breaks in the KRT5 gene, followed by non-homologous end joining (NHEJ) repair that typically results in disruptive mutations. The resultant knockout cell lines exhibit clear phenotypic alterations such as changes in cell adhesion, proliferation rates, and survival under stress conditions, thus proving invaluable for studies on epithelial cell biology.
The scientific importance of KRT5 Gene Knockout Cell Lines extends to their applications in both basic research and clinical settings. They serve as powerful tools for studying keratinocyte differentiation, epidermal development, and pathogenesis of skin diseases, including disorders like epidermolysis bullosa or squamous cell carcinoma. Additionally, these knockout models can aid in testing potential therapeutic approaches targeting KRT5-related pathways.
One of the primary advantages of our KRT5 Gene Knockout Cell Lines is the precision of our knockout methodology compared to traditional methodologies such as chemical mutagenesis, which can result in off-target effects and less reproducible outcomes. Furthermore, our lines are rigorously validated for KRT5 disruption, ensuring that researchers utilize a reliable model.
For researchers, clinicians, and pharmaceutical developers focused on skin biology and pathology, these knockout cell lines provide a robust platform for advancing knowledge and therapeutics in dermatology and oncology. Our company prides itself on its extensive expertise in gene editing and cell line development, offering high-quality products that facilitate cutting-edge scientific research.
Please note that all services are for research use only. Not intended for any clinical use.
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