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WDR19 Knockout Cell Lines

Gene: WDR19

Official Full Name: WD repeat domain 19provided by HGNC

Gene Summary: The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by glycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO12614 WDR19 Knockout cell line (HeLa) Human WDR19 1:3~1:6 Negative Online Inquiry
KO12615 WDR19 Knockout cell line (HCT 116) Human WDR19 1:2~1:4 Negative Online Inquiry
KO12616 WDR19 Knockout cell line (HEK293) Human WDR19 1:3~1:6 Negative Online Inquiry
KO12617 WDR19 Knockout cell line (A549) Human WDR19 1:3~1:4 Negative Online Inquiry

Background

WDR19 Gene Knockout Cell Lines are genetically engineered cell lines designed to study the functional role of the WDR19 gene, which encodes a protein involved in cilia assembly and cellular signaling pathways. These knockout cell lines are created using advanced CRISPR-Cas9 gene editing technology that effectively disrupts the WDR19 gene's sequence, resulting in the loss of its expression. As a consequence, researchers can examine the phenotypic changes that occur due to the absence of this gene, providing valuable insights into various biological processes such as developmental biology, ciliopathies, and cell cycle regulation.

The key function of the WDR19 gene is its role in the assembly and maintenance of primary cilia, which are crucial sensory organelles responsibe for mediating critical signaling pathways, including Hedgehog and Wnt signaling. By utilizing these knockout cell lines, researchers can investigate the implications of disrupted ciliary function on cellular behavior, disease mechanisms, and potential therapeutic targets in conditions such as polycystic kidney disease, Bardet-Biedl syndrome, and other ciliopathies.

In terms of scientific importance, WDR19 Gene Knockout Cell Lines offer substantial utility in both basic and applied research settings. Their use allows for high-throughput screening of drug candidates, elucidation of gene function, and validation of disease mechanisms. The specific advantages of these knockout lines include their reproducibility, ease of use, and clear genotype-phenotype relationships, making them superior to traditional knockdown techniques that may produce off-target effects.

Researchers and clinicians will find these WDR19 Gene Knockout Cell Lines to be invaluable in their explorations of genetic regulation and disease modeling. The precision of CRISPR technology ensures reliable and consistent results, which not only accelerates the research process but also enhances the potential for significant breakthroughs in understanding ciliary function and related diseases.

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

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