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PPP3CB Knockout Cell Lines

Gene: PPP3CB

Official Full Name: protein phosphatase 3 catalytic subunit betaprovided by HGNC

Gene Summary: Enables several functions, including calmodulin binding activity; calmodulin-dependent protein phosphatase activity; and protein phosphatase 2B binding activity. Involved in several processes, including calcineurin-NFAT signaling cascade; positive regulation of lysosome organization; and positive regulation of protein localization to nucleus. Located in cytoplasm. Part of calcineurin complex. Implicated in aortic valve stenosis. Biomarker of focal segmental glomerulosclerosis and schizophrenia. [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
KO01030 PPP3CB Knockout cell line (HEK293) Human PPP3CB 1:3~1:6 Negative Online Inquiry
KO10549 PPP3CB Knockout cell line (HeLa) Human PPP3CB 1:3~1:6 Negative Online Inquiry
KO10550 PPP3CB Knockout cell line (HCT 116) Human PPP3CB 1:2~1:4 Negative Online Inquiry
KO10551 PPP3CB Knockout cell line (A549) Human PPP3CB 1:3~1:4 Negative Online Inquiry

Background

PPP3CB Gene Knockout Cell Lines are specifically engineered cellular models designed to facilitate the study of the PPP3CB gene, which encodes the regulatory subunit of the calcium/calmodulin-dependent protein phosphatase, calcineurin. These cell lines have had their PPP3CB gene disrupted, thereby enabling researchers to dissect the functional roles of this molecule in various biological processes, including T-cell activation, neuronal signaling, and cardiac hypertrophy.

The primary function of these knockout cell lines is to serve as a powerful tool for elucidating the downstream signaling pathways and physiological implications of calcineurin activity. By assessing cellular responses in the absence of PPP3CB, researchers can gain insight into the mechanisms underlying diseases where calcineurin is implicated, such as autoimmune disorders and neurodegenerative diseases. The targeted gene disruption allows researchers to confidently attribute observed phenotypic changes to the lack of PPP3CB expression.

The scientific importance of PPP3CB Gene Knockout Cell Lines extends into both research and clinical settings. These cell models are pivotal for drug discovery efforts, particularly in screening compounds that may modulate calcineurin pathways for therapeutic benefits. Additionally, they hold potential for advancing our understanding of diseases linked to calcium signaling dysregulation.

Compared to traditional models or other gene editing techniques, knockout cell lines provide consistent and reproducible variants with clear genetic backgrounds, minimizing variability and enhancing the reliability of experimental outcomes. Furthermore, the specificity of the gene knockout ensures that researchers can investigate the precise role of the PPP3CB in a focused manner, allowing for targeted research that can lead to significant advancements in treatment options.

For researchers and clinicians focused on the intersections of cellular signaling, immunology, and developmental biology, PPP3CB Gene Knockout Cell Lines offer indispensable tools for understanding complex biological mechanisms. Our company prides itself on delivering high-quality, validated biological products backed by rigorous scientific research, ensuring that our clients have dependable resources to support their innovative work in the field.

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

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