Gene: PKP2
Official Full Name: plakophilin 2provided by HGNC
Gene Summary: This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This gene may regulate the signaling activity of beta-catenin and is required to maintain transcription of genes that control intracellular calcium cycling including ryanodine receptor 2, ankyrin-B, triadin, and calcium channel, voltage-dependent, L type, alpha 1C. Mutations in this gene are associated with different inherited cardiac conditions including Arrythmogenic Cardiomyopathy, Brugada Syndrome, and Idiopathic Ventricular Fibrillation. A processed pseudogene with high similarity to this gene has been mapped to chromosome 12p13. [provided by RefSeq, May 2022]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36056 | PKP2 Knockout cell line (HeLa) | Human | PKP2 | 1:3~1:6 | Negative | Online Inquiry |
KO36057 | PKP2 Knockout cell line (HCT 116) | Human | PKP2 | 1:2~1:4 | Negative | Online Inquiry |
KO36058 | PKP2 Knockout cell line (HEK293) | Human | PKP2 | 1:3~1:6 | Negative | Online Inquiry |
KO36059 | PKP2 Knockout cell line (A549) | Human | PKP2 | 1:3~1:4 | Negative | Online Inquiry |
PKP2 Gene Knockout Cell Lines are specialized cellular models designed to facilitate the in-depth study of the plakophilin-2 (PKP2) gene, which plays a crucial role in cellular adhesion and cardiac integrity. These cell lines have undergone a targeted gene knockout, resulting in the disruption of PKP2 expression. This innovative tool enables researchers to investigate the molecular pathways influenced by PKP2 and to assess its impact on cellular behavior in both physiological and pathological contexts.
The key function of PKP2 Gene Knockout Cell Lines lies in their ability to provide a controlled environment for examining the consequences of PKP2 loss on cell-cell junctions, particularly in cardiac myocytes. By leveraging these knockout models, scientists can elucidate the mechanisms associated with arrhythmogenic right ventricular cardiomyopathy (ARVC) and other cardiac-related disorders linked to PKP2 mutations. The deletion of this critical gene allows an accurate assessment of the molecular cascades and phenotypic alterations that result from its absence, leading to profound insights into heart physiology and disease.
The scientific importance of PKP2 Gene Knockout Cell Lines is underscored by their applications in both basic research and clinical settings. These models serve as a foundation for drug discovery, genetic therapy studies, and mechanistic investigations, greatly contributing to our understanding of cardiomyopathies and related diseases. Furthermore, the results obtained from these cell lines could pave the way for the development of targeted therapies aimed at restoring normal function in cardiac tissues.
Distinctive advantages of the PKP2 Gene Knockout Cell Lines include their highly specific-genetic alteration, reproducibility, and the accompanying characterization data provided. Compared to alternative methods such as siRNA knockdown techniques or standard cell lines, these knockout lines offer a permanent solution for studying the loss-of-function phenotypes, ensuring that researchers can rely on consistent results over extended experimental periods.
The value of PKP2 Gene Knockout Cell Lines to researchers and clinicians is multifaceted. With these tools, they can accelerate their understanding of disease mechanisms, assess potential treatments, and uncover novel insights that have significant implications for the field of cardiovascular research. Furthermore, our company is committed to excellence in the development of innovative biological products, providing comprehensive support and expertise to ensure your research needs are met with precision and quality. Our advent into gene knockout technologies reflects our dedication to advancing scientific discovery and driving impactful research outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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