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OCLN Knockout Cell Lines

Gene: OCLN

Official Full Name: occludinprovided by HGNC

Gene Summary: This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO20345 OCLN Knockout cell line (HeLa) Human OCLN 1:3~1:6 Negative Online Inquiry
KO20346 OCLN Knockout cell line (HCT 116) Human OCLN 1:2~1:4 Negative Online Inquiry
KO20347 OCLN Knockout cell line (HEK293) Human OCLN 1:3~1:6 Negative Online Inquiry
KO20348 OCLN Knockout cell line (A549) Human OCLN 1:3~1:4 Negative Online Inquiry

Background

OCLN Gene Knockout Cell Lines are genetically engineered cell lines that have undergone targeted disruption of the occludin (OCLN) gene, which encodes a crucial component of tight junctions in epithelial cells. These cell lines provide researchers with a powerful tool to investigate the role of occludin in barrier function, cell signaling, and a variety of physiological and pathological processes, such as inflammation and cancer metastasis.

The key mechanism through which OCLN gene knockout cell lines operate involves the complete ablation of occludin expression, leading to alterations in tight junction assembly and function. Consequently, this results in changes to transcellular transport, permeability, and cell-cell adhesion. Researchers can utilize these cell lines to better understand how occludin contributes to cellular homeostasis and how its dysregulation can lead to various diseases.

Scientifically, OCLN gene knockout cell lines are invaluable for both academic and clinical research, offering insights into the pathophysiology of disorders related to epithelial barrier dysfunction, such as inflammatory bowel disease, neurodegenerative disorders, and cancer progression. They are particularly useful in drug discovery and development, allowing researchers to screen potential therapeutic agents aimed at modulating tight junction integrity.

Compared to traditional cell lines, which express occludin, OCLN gene knockout cell lines eliminate confounding variables, allowing for clearer and more specific analysis of occludin's biological roles. This specificity enhances reproducibility and reliability in experimental results.

For researchers and clinicians seeking to unravel the complexities of epithelial biology, these knockout cell lines represent an essential resource. They enable the dissection of occludin's contributions to various cellular processes and disease mechanisms. Our company specializes in providing cutting-edge biological products, ensuring that our clients have access to the highest quality resources for their research needs.

Please note that all services are for research use only. Not intended for any clinical use.

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