Gene: CACNA1H
Official Full Name: calcium voltage-gated channel subunit alpha1 Hprovided by HGNC
Gene Summary: This gene encodes a T-type member of the alpha-1 subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. The alpha-1 subunit has 24 transmembrane segments and forms the pore through which ions pass into the cell. There are multiple isoforms of each of the proteins in the complex, either encoded by different genes or the result of alternative splicing of transcripts. Alternate transcriptional splice variants, encoding different isoforms, have been characterized for the gene described here. Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE). [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO10914 | CACNA1H Knockout cell line (HCT 116) | Human | CACNA1H | 1:2~1:4 | Negative | Online Inquiry |
KO10915 | CACNA1H Knockout cell line (HEK293) | Human | CACNA1H | 1:3~1:6 | Negative | Online Inquiry |
KO10916 | CACNA1H Knockout cell line (A549) | Human | CACNA1H | 1:3~1:4 | Negative | Online Inquiry |
CACNA1H Gene Knockout Cell Lines are specialized cellular models created through the targeted disruption of the CACNA1H gene, which encodes for the α1H subunit of the T-type calcium channel. These cell lines are invaluable tools for studying the physiological and pathological roles of calcium signaling pathways, particularly in the context of neuronal excitability and pain mechanisms. The knockout of this gene results in the absence of functional T-type calcium channels, allowing for the detailed investigation of calcium's role in various cellular processes, including neurotransmitter release, muscle contraction, and the modulation of neuronal activity.
The key function of these knockout cell lines lies in their ability to elucidate the specific contributions of T-type calcium channels in maintaining cellular homeostasis and mediating responses to pharmacological agents. Research utilizing CACNA1H gene knockout models has yielded significant insights into conditions such as epilepsy, chronic pain, and cardiovascular disorders, where aberrant calcium signaling is implicated. In clinical settings, these models are essential for validating potential drug targets, thereby accelerating the development of novel therapeutic strategies that modulate calcium channel activity.
Compared to traditional cell lines that express the CACNA1H gene, these knockout models provide a clear advantage by enabling the direct correlation between calcium channel activity and phenotypic outcomes. Researchers benefit from the specificity of the knockout, which minimizes confounding effects from other calcium channels, allowing for precise experimental designs.
By utilizing CACNA1H Gene Knockout Cell Lines, researchers and clinicians have access to a powerful platform for advancing our understanding of calcium signaling mechanisms involved in diseases. With these insights, the development of targeted interventions could lead to improved treatment options for patients suffering from calcium channel-related disorders.
At our company, we specialize in providing high-quality biological products tailored for cutting-edge research. Our expertise in cell line development and gene targeting ensures that our cell lines, including the CACNA1H Gene Knockout variations, meet the rigorous standards required for impactful scientific discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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