Gene: KRT13
Official Full Name: keratin 13provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This type I cytokeratin is paired with keratin 4 and expressed in the suprabasal layers of non-cornified stratified epithelia. Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus. The type I cytokeratins are clustered in a region of chromosome 17q21.2. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been described. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36878 | KRT13 Knockout cell line (HeLa) | Human | KRT13 | 1:3~1:6 | Negative | Online Inquiry |
KO36879 | KRT13 Knockout cell line (HCT 116) | Human | KRT13 | 1:2~1:4 | Negative | Online Inquiry |
KRT13 Gene Knockout Cell Lines are genetically engineered cell lines in which the keratin 13 (KRT13) gene has been deliberately disrupted. Keratin 13 plays a pivotal role in the structural integrity of epithelial cells, contributing to the formation of intermediate filaments in various tissues, particularly in stratified epithelia. By knocking out this gene, researchers can investigate the resulting biological changes, thus providing insights into its physiological roles and relevance in diseases such as epidermolysis bullosa or squamous cell carcinoma.
The primary function of KRT13 Gene Knockout Cell Lines is to enable the study of keratin-associated cellular processes without the confounding effects of the KRT13 gene expression. This is achieved through advanced CRISPR-Cas9 gene editing technology that ensures precise and efficient gene disruption. The resultant cell lines serve as invaluable tools in dissecting the molecular pathways involved in keratinization, cellular stress responses, and differentiation processes.
Scientifically, these cell lines are critical for both fundamental research and translational applications. They allow researchers to model disease states, screen for potential therapeutics, and evaluate therapeutic responses in a controlled environment. Furthermore, their utility extends to drug discovery and testing, wherein the altered cellular dynamics can reveal new insights into drug interactions and efficacy.
Compared to traditional cell lines, KRT13 Gene Knockout Cell Lines offer a unique advantage of being specifically tailored for studies focused on keratin biology. As alternative models may not accurately replicate the loss-of-function scenarios presented by KRT13 knockout, these specialized lines provide a more authentic representation of pathological conditions associated with keratin disruptions.
For researchers, clinicians, and biotechnology companies working on skin biology or related pathologies, KRT13 Gene Knockout Cell Lines present a powerful and precise tool that can facilitate groundbreaking discoveries. Our company's expertise in genetic engineering and cell line development ensures the highest quality and reliability in these models, positioning us at the forefront of innovations in biological research solutions. We are committed to supporting scientific advancements and enhancing the understanding of complex biological mechanisms.
Please note that all services are for research use only. Not intended for any clinical use.
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