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KCNK2 Knockout Cell Lines

Gene: KCNK2

Official Full Name: potassium two pore domain channel subfamily K member 2provided by HGNC

Gene Summary: This gene encodes one of the members of the two-pore-domain background potassium channel protein family. This type of potassium channel is formed by two homodimers that create a channel that leaks potassium out of the cell to control resting membrane potential. The channel can be opened, however, by certain anesthetics, membrane stretching, intracellular acidosis, and heat. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02312 KCNK2 Knockout cell line (HeLa) Human KCNK2 1:3~1:6 Negative Online Inquiry

Background

KCNK2 Gene Knockout Cell Lines are genetically engineered models specifically designed to investigate the physiological roles and functional mechanisms of the KCNK2 gene, which encodes a potassium channel involved in regulating cellular excitability and ion homeostasis. By providing a system where KCNK2 expression is precisely disrupted, these cell lines offer a robust platform for studying the downstream effects of potassium channel dysfunction, which can have significant implications in various physiological and pathological contexts, such as neuronal signaling, cardiac function, and smooth muscle contraction.

The primary function of these knockout cell lines is to enable researchers to explore the absence of KCNK2. The mechanism involves a deliberate introduction of mutations to the gene, thereby preventing the synthesis of functional KCNK2 protein. This knockout allows for comprehensive studies on cellular behavior in response to altered ionic currents, revealing the potential role of KCNK2 in diseases such as epilepsy, arrhythmias, and hyperaldosteronism.

The scientific importance of KCNK2 Gene Knockout Cell Lines lies in their wide-ranging applications in both research and clinical settings. Researchers can use these models to uncover pathways involved in excitability and signaling, aiding in the development of therapeutic interventions targeting KCNK2-related dysfunctions. Furthermore, these cell lines are invaluable in drug discovery and screening, allowing scientists to test the efficacy of novel therapeutics on ionic channel modulation.

Compared to alternative methods, such as transient knockdown approaches, these knockout cell lines provide stable, reproducible results that facilitate long-term studies and allow for high-throughput screening. Users benefit from the rigor and consistency these models offer, thereby enhancing experimental validity.

For researchers, clinicians, and biotech companies, the KCNK2 Gene Knockout Cell Lines present a strategic tool that aligns with the urgency of advancing our understanding of ion channel biology. Their robust functionality and experimental reliability make them essential for unlocking the complexities of cellular excitability and the development of targeted therapies.

Our company specializes in cutting-edge genetic models and maintains a commitment to providing researchers with the highest quality products. With extensive expertise in developing and characterizing genetic tools, we stand at the forefront of innovation, ensuring our offerings meet the evolving needs of the scientific community.

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

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