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KCNQ5 Knockout Cell Lines

Gene: KCNQ5

Official Full Name: potassium voltage-gated channel subfamily Q member 5provided by HGNC

Gene Summary: This gene is a member of the KCNQ potassium channel gene family that is differentially expressed in subregions of the brain and in skeletal muscle. The protein encoded by this gene yields currents that activate slowly with depolarization and can form heteromeric channels with the protein encoded by the KCNQ3 gene. Currents expressed from this protein have voltage dependences and inhibitor sensitivities in common with M-currents. They are also inhibited by M1 muscarinic receptor activation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO16825 KCNQ5 Knockout cell line (HEK293) Human KCNQ5 1:3~1:6 Negative Online Inquiry
KO16826 KCNQ5 Knockout cell line (A549) Human KCNQ5 1:3~1:4 Negative Online Inquiry

Background

KCNQ5 Gene Knockout Cell Lines are genetically engineered cell lines in which the KCNQ5 gene has been deliberately disrupted or "knocked out." This gene encodes a subunit of the potassium ion channel, which plays a critical role in regulating neuronal excitability and synaptic plasticity in the central nervous system. The knockout of KCNQ5 allows researchers to investigate the physiological and pathological roles of this ion channel in various cellular processes and disease models.

The primary mechanism of these cell lines involves the absence of functional KCNQ5 protein, leading to altered ion channel activity that can impact cellular excitability and signaling. This alteration enables scientists to explore the specific contributions of KCNQ5 to disorders such as epilepsy, neurodevelopmental conditions, and other neurophysiological disorders associated with ion channel dysfunction. By utilizing these cell lines, researchers can study the resulting phenotypic changes that emerge from KCNQ5 deficiency, including alterations in action potential firing, synaptic transmission, and cellular responses to pharmacological agents.

The scientific importance of KCNQ5 Gene Knockout Cell Lines lies in their application in both fundamental research and clinical contexts. They serve as valuable models for understanding the intricate dynamics of ion channel physiology and the implications of their malfunction in disease states. These models can facilitate drug discovery, enabling the development of targeted therapies that modulate KCNQ channel activity, thereby addressing specific patient needs.

What sets our KCNQ5 Gene Knockout Cell Lines apart from other available models is their high specificity and rigorously validated genetic modifications, ensuring reliability and reproducibility in experimental outcomes. Additionally, our cell lines are generated using state-of-the-art CRISPR/Cas9 technology, ensuring precise editing that minimizes off-target effects.

For researchers and clinicians, these cell lines represent a crucial tool for advancing knowledge in neurobiology and developing novel therapeutic strategies. By investing in our KCNQ5 Gene Knockout Cell Lines, users gain access to a resource that not only enhances their research capabilities but also accelerates the pursuit of breakthroughs in understanding and treating ion channel-related disorders. Our company prides itself on its commitment to excellence in biological products, supported by a team of experts in genetic engineering and cell biology, ensuring the highest standards of quality and innovation in the scientific community.

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

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