Gene: CACNB4
Official Full Name: calcium voltage-gated channel auxiliary subunit beta 4provided by HGNC
Gene Summary: This gene encodes a member of the beta subunit family of voltage-dependent calcium channel complex proteins. 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. Various versions of each of these subunits exist, either expressed from similar genes or the result of alternative splicing. The protein encoded by this locus plays an important role in calcium channel function by modulating G protein inhibition, increasing peak calcium current, controlling the alpha-1 subunit membrane targeting and shifting the voltage dependence of activation and inactivation. Certain mutations in this gene have been associated with idiopathic generalized epilepsy (IGE), juvenile myoclonic epilepsy (JME), and episodic ataxia, type 5. [provided by RefSeq, Aug 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO10899 | CACNB4 Knockout cell line (HeLa) | Human | CACNB4 | 1:3~1:6 | Negative | Online Inquiry |
KO10900 | CACNB4 Knockout cell line (HCT 116) | Human | CACNB4 | 1:2~1:4 | Negative | Online Inquiry |
KO10901 | CACNB4 Knockout cell line (HEK293) | Human | CACNB4 | 1:3~1:6 | Negative | Online Inquiry |
CACNB4 Gene Knockout Cell Lines are genetically modified cell lines in which the CACNB4 gene has been specifically disrupted or rendered non-functional. This gene, which encodes for the beta-4 subunit of voltage-gated calcium channels, plays a crucial role in various cellular processes, including muscle contraction, neurotransmitter release, and calcium-mediated signal transduction. By producing these knockout cell lines, researchers gain valuable tools to study the functional implications of CACNB4 loss, facilitating deeper insights into pathological conditions associated with calcium dysregulation.
The primary mechanism of action involves the complete ablation of CACNB4 expression, leading to diminished calcium channel functionality. This knockout results in alterations to intracellular calcium levels, subsequently affecting signaling pathways critical for cellular responses. Researchers utilize these cell lines to elucidate the molecular mechanisms underlying a variety of diseases, such as certain cardiovascular dysfunctions and neurological disorders, where aberrant calcium signaling is implicated.
The scientific importance of CACNB4 Gene Knockout Cell Lines is evident in both basic research and clinical applications. They serve as models for testing pharmacological interventions aimed at restoring calcium homeostasis, offering a platform for drug discovery and efficacy evaluation. Furthermore, they are invaluable for studying gene interactions and signaling cascades influenced by calcium dynamics, which can translate into new therapeutic strategies.
The specific advantages of utilizing CACNB4 Gene Knockout Cell Lines include their high specificity and reliability, as well as the ability to generate reproducible results unmatched by alternative methods such as siRNA knockdown or soluble inhibitors. These knockout models provide a stable and long-term approach to investigate the involvement of CACNB4 without the confounding effects observed in transient manipulations.
Researchers and clinicians focused on calcium signaling pathways will find these cell lines indispensable due to their distinct adaptability for various experimental designs. They enable detailed explorations into the biochemical and molecular underpinnings of diseases, enhancing the development of targeted therapies.
At [Your Company Name], we pride ourselves on our commitment to advancing scientific research through premium biological products. Our expertise in genetic engineering ensures that we provide cell lines of the highest quality, empowering researchers to unlock new frontiers in understanding calcium biology and its implications in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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