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DUSP12 Knockout Cell Lines

Gene: DUSP12

Official Full Name: dual specificity phosphatase 12provided by HGNC

Gene Summary: The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product is the human ortholog of the Saccharomyces cerevisiae YVH1 protein tyrosine phosphatase. It is localized predominantly in the nucleus, and is novel in that it contains, and is regulated by a zinc finger domain. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO31010 DUSP12 Knockout cell line (HeLa) Human DUSP12 1:3~1:6 Negative Online Inquiry
KO31011 DUSP12 Knockout cell line (HCT 116) Human DUSP12 1:2~1:4 Negative Online Inquiry
KO31012 DUSP12 Knockout cell line (HEK293) Human DUSP12 1:3~1:6 Negative Online Inquiry
KO31013 DUSP12 Knockout cell line (A549) Human DUSP12 1:3~1:4 Negative Online Inquiry

Background

DUSP12 Gene Knockout Cell Lines are a specialized tool designed for the study of dual specificity protein phosphatase 12 (DUSP12), providing researchers with a vital resource for investigating its role in cellular signaling pathways and disease states. These cell lines are engineered via CRISPR/Cas9 technology to abrogate the expression of the DUSP12 gene, resulting in a standardized model that allows for the dissection of its physiological functions and interactions.

The key function of DUSP12 lies in its ability to dephosphorylate specific mitogen-activated protein kinases (MAPKs), thereby regulating key signaling cascades that influence cell proliferation, differentiation, and apoptosis. By utilizing the DUSP12 knockout cell lines, researchers can precisely elucidate the downstream effects of manipulating DUSP12 activity, offering insights into its contributions to various biological processes and pathologies, including cancer and inflammation.

The scientific importance of DUSP12 gene knockout cell lines is underscored by their potential applications in both basic research and clinical settings. They serve as invaluable models for studying MAPK signaling in relation to disease mechanisms, drug response, and therapeutic development. This characterization is essential for pharmaceutical research, where targeting DUSP12 can provide novel strategies in cancer therapies, potentially leading to more effective treatment regimens.

Compared to traditional methods that may involve less precise gene editing or varied cellular contexts, the DUSP12 knockout model stands out for its reliability, reproducibility, and enhanced specificity. This makes it an ideal choice for researchers seeking to validate their findings or develop new hypotheses involving DUSP12 signaling pathways.

In essence, the DUSP12 Gene Knockout Cell Lines represent a critical innovation for scientific inquiry, equipping researchers and clinicians with the tools necessary to advance our understanding of complex biological systems. Backed by our company's extensive expertise in genetic engineering and cell line development, we are committed to providing cutting-edge solutions that empower scientific discovery and foster advancements in health and medicine.

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

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