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WASHC2C Knockout Cell Lines

Gene: WASHC2C

Official Full Name: WASH complex subunit 2Cprovided by HGNC

Gene Summary: Enables phosphatidylinositol phosphate binding activity; phosphatidylinositol-3,4-bisphosphate binding activity; and retromer complex binding activity. Involved in several processes, including endosomal transport; negative regulation of barbed-end actin filament capping; and protein localization to endosome. Located in cytosol; early endosome; and nucleolus. Part of WASH complex. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO21215 WASHC2C Knockout cell line (HeLa) Human WASHC2C 1:3~1:6 Negative Online Inquiry
KO21216 WASHC2C Knockout cell line (HCT 116) Human WASHC2C 1:2~1:4 Negative Online Inquiry
KO21217 WASHC2C Knockout cell line (HEK293) Human WASHC2C 1:3~1:6 Negative Online Inquiry
KO21218 WASHC2C Knockout cell line (A549) Human WASHC2C 1:3~1:4 Negative Online Inquiry

Background

WASHC2C Gene Knockout Cell Lines are genetically modified cell lines specifically engineered to lack the WASH complex subunit WASHC2C. These cell lines serve as essential tools for studying the biological functions of WASHC2C and its role in cellular processes such as endosomal sorting, cellular trafficking, and regulation of cytoskeletal dynamics. By creating a knockout cell line, researchers can effectively elucidate the phenotype associated with the absence of this gene, providing insights into its contributions to various cellular mechanisms and pathways.

The key mechanism of action involves the disruption of the WASH complex, a crucial regulator in the actin cytoskeleton remodeling during endosomal transport. The absence of WASHC2C leads to impaired endosomal dynamics and can affect vesicle formation, trafficking, and recycling, thus enabling researchers to investigate how these alterations impact cellular homeostasis, signal transduction, and overall cell health.

The scientific importance of WASHC2C Gene Knockout Cell Lines is profound, as they allow for the exploration of cellular dysfunctions associated with diseases, including cancer and neurodegenerative disorders. Their applications extend to both research and clinical settings, where they can facilitate drug screening and gene therapy studies targeting WASHC2C-related pathways.

Compared to conventional wild-type cell lines, the uniqueness of these knockout lines lies in their ability to provide a more accurate representation of the pathological states induced by WASHC2C deficiency. This specificity enhances experimental reproducibility and robustness, offering researchers a superior model system to unravel the complexities of cellular behavior.

For researchers and clinicians focused on the intersections of cellular biology and disease pathology, these cell lines offer invaluable insights that can lead to transformative discoveries and therapeutic advancements. With our extensive expertise in genetic engineering and cell line development, we are committed to delivering high-quality biological products that empower scientific innovation and facilitate breakthroughs in the study of disease mechanisms.

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

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