Gene: GJB3
Official Full Name: gap junction protein beta 3provided by HGNC
Gene Summary: This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37655 | GJB3 Knockout cell line (HeLa) | Human | GJB3 | 1:3~1:6 | Negative | Online Inquiry |
KO37656 | GJB3 Knockout cell line (HCT 116) | Human | GJB3 | 1:2~1:4 | Negative | Online Inquiry |
KO37657 | GJB3 Knockout cell line (A549) | Human | GJB3 | 1:3~1:4 | Negative | Online Inquiry |
GJB3 Gene Knockout Cell Lines are precisely engineered cellular models that lack the expression of the GJB3 gene, which encodes a key protein involved in gap junction intercellular communication. These cell lines utilize advanced CRISPR/Cas9 or similar genome-editing technologies to induce targeted mutations that abolish GJB3 gene function, thereby facilitating investigation into its biological roles and associated disease mechanisms.
The primary function of GJB3 is to encode the gap junction protein connexin 31, which plays a critical role in cellular communication, particularly in the skin and other epithelial tissues. By studying these knockout cell lines, researchers can explore the downstream effects of perturbed cell signaling pathways, providing insights into conditions such as skin disorders and hearing impairments related to GJB3 mutations. The precise deletion allows for the assessment of phenotypic changes and the biological relevance of GJB3 in various physiological contexts.
From a scientific perspective, GJB3 Gene Knockout Cell Lines serve as invaluable tools in both basic and translational research. They enhance our understanding of gap junction functionality and allow researchers to develop targeted therapies for conditions associated with GJB3 dysfunction. In clinical settings, these models can be pivotal for drug discovery processes, optimizing treatment approaches that target specific molecular pathways.
What sets our GJB3 Gene Knockout Cell Lines apart from alternatives is the high specificity and efficiency of the knockout process, ensuring minimal off-target effects. Additionally, our cell lines come with robust characterization data, providing confidence in their use for research applications. Researchers can also benefit from our comprehensive support, including troubleshooting and application guidance, which is integral to their experimental design.
Our expertise in recombinant technologies, coupled with a commitment to quality and consistency, positions our company as a leader in providing advanced biological products. We understand the nuances of gene editing and are dedicated to empowering the scientific community with innovative tools that drive impactful research and discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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