Gene: HCN3
Official Full Name: hyperpolarization activated cyclic nucleotide gated potassium channel 3provided by HGNC
Gene Summary: This gene encodes a multi-pass membrane protein that functions as a voltage gated cation channel. The encoded protein is a member of a family of closely related cyclic adenosine monophosphate-binding channel proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO17158 | HCN3 Knockout cell line (HeLa) | Human | HCN3 | 1:3~1:6 | Negative | Online Inquiry |
KO17159 | HCN3 Knockout cell line (HCT 116) | Human | HCN3 | 1:2~1:4 | Negative | Online Inquiry |
KO17160 | HCN3 Knockout cell line (HEK293) | Human | HCN3 | 1:3~1:6 | Negative | Online Inquiry |
KO17161 | HCN3 Knockout cell line (A549) | Human | HCN3 | 1:3~1:4 | Negative | Online Inquiry |
HCN3 Gene Knockout Cell Lines are specialized cell lines engineered to ablate the expression of the HCN3 gene, which encodes for hyperpolarization-activated cyclic nucleotide-gated (HCN) channels. These ion channels play significant roles in excitatory and regulatory functions within various types of neurons. By knocking out the HCN3 gene, these cell lines provide researchers with a vital tool for studying the specific contributions of HCN3 in cellular excitability, synaptic transmission, and overall neuronal functionality.
The primary function of HCN3 gene knockout cell lines lies in their ability to model the physiological and pathophysiological roles of HCN3 channels. The absence of this specific ion channel alters the cellular ionic environment, enabling investigations into how HCN3 influences resting membrane potential, action potential firing, and neurotransmitter release. With advancements in CRISPR-Cas9 technology, these knockout models allow for precise gene editing, facilitating high-throughput studies in electrophysiology and pharmacology.
From a scientific perspective, HCN3 knockout cell lines are crucial in understanding not just fundamental electrophysiological mechanisms, but also their implications in neurological conditions such as epilepsy, mood disorders, and cardiac arrhythmias. Their application extends to drug discovery processes, where the characterization of novel pharmacological agents can benefit from the absence of HCN3-mediated currents.
One distinct advantage of HCN3 gene knockout cell lines compared to traditional pharmacological approaches is the ability to study the gene’s impact without confounding factors associated with the use of blockers or inhibitors. This targeted approach provides a more accurate representation of cellular behavior, enhancing the reliability of research findings.
For researchers and clinicians focused on neuronal physiology or drug development, HCN3 gene knockout cell lines are invaluable. Their capability to elucidate gene-specific roles offers insights that can translate into therapeutic strategies and enhance understanding of neuronal function.
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