Gene: COL17A1
Official Full Name: collagen type XVII alpha 1 chainprovided by HGNC
Gene Summary: This gene encodes the alpha chain of type XVII collagen. Unlike most collagens, collagen XVII is a transmembrane protein. Collagen XVII is a structural component of hemidesmosomes, multiprotein complexes at the dermal-epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane. Mutations in this gene are associated with both generalized atrophic benign and junctional epidermolysis bullosa. Two homotrimeric forms of type XVII collagen exist. The full length form is the transmembrane protein. A soluble form, referred to as either ectodomain or LAD-1, is generated by proteolytic processing of the full length form. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05966 | COL17A1 Knockout cell line (HCT 116) | Human | COL17A1 | 1:2~1:4 | Negative | Online Inquiry |
KO05967 | COL17A1 Knockout cell line (HEK293) | Human | COL17A1 | 1:3~1:6 | Negative | Online Inquiry |
KO05968 | COL17A1 Knockout cell line (A549) | Human | COL17A1 | 1:3~1:4 | Negative | Online Inquiry |
COL17A1 Gene Knockout Cell Lines are specialized cellular models created through the targeted gene-disruption technique, specifically designed to investigate the functions and pathological implications of the COL17A1 gene, which encodes for type XVII collagen. This protein plays a crucial role in maintaining the integrity of epithelial tissues and is particularly significant in skin and ocular health. By knocking out the COL17A1 gene, researchers can simulate various pathological conditions, facilitating the study of disorders such as epidermolysis bullosa, a disease characterized by skin fragility and blistering.
These knockout cell lines function by utilizing CRISPR/Cas9 technology, a precise and efficient method for inducing targeted genetic modifications. Once the COL17A1 gene has been deactivated, resulting cell lines exhibit alterations in collagen structure, adhesion properties, and signaling pathways related to cell stress and repair mechanisms. This provides an invaluable platform for studying the molecular pathways and interactions influenced by COL17A1 deficiency.
From a scientific perspective, COL17A1 Gene Knockout Cell Lines hold immense significance in both research and clinical settings. They serve as vital tools for drug development, pathophysiological studies, and potential therapeutic interventions aimed at treating collagen-related disorders. Furthermore, these models can aid in high-throughput screening for new compounds that can restore normal cellular functions disrupted by the absence of COL17A1.
Compared to traditional cell lines or other genetically modified models, COL17A1 Gene Knockout Cell Lines offer unparalleled specificity and relevance to human disease mechanisms. Their unique ability to mimic the physiological environment of diseased tissues ensures that findings are more translatable to actual clinical situations, providing researchers and clinicians with robust data for developing innovative therapies.
The value of COL17A1 Gene Knockout Cell Lines is further accentuated by their contribution to advancing our understanding of dermal health and disease, ultimately guiding more effective treatments for patients. Our company is dedicated to providing high-quality biological products and expert solutions, empowering researchers and healthcare professionals to enhance their work and contribute to groundbreaking discoveries within the field of molecular biology and regenerative medicine.
Please note that all services are for research use only. Not intended for any clinical use.
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