Gene: KLHL12
Official Full Name: kelch like family member 12provided by HGNC
Gene Summary: This gene encodes a member of the KLHL (Kelch-like) family of proteins. This protein has been identified as an autoantigen in the autoimmune disease Sjogren's syndrome and as a potential biomarker in primary biliary cirrhosis. This protein may act as a substrate adaptor of the Cullin-3 ubiquitin ligase complex to promote substrate-specific ubiquitylation. Ubiquitylation by this complex has been shown to regulate the Wnt signaling pathway as well as COPII vesicle coat size. A pseudogene has been identified on chromosome 22. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20151 | KLHL12 Knockout cell line (HeLa) | Human | KLHL12 | 1:3~1:6 | Negative | Online Inquiry |
KO20152 | KLHL12 Knockout cell line (HCT 116) | Human | KLHL12 | 1:2~1:4 | Negative | Online Inquiry |
KO20153 | KLHL12 Knockout cell line (HEK293) | Human | KLHL12 | 1:3~1:6 | Negative | Online Inquiry |
KO20154 | KLHL12 Knockout cell line (A549) | Human | KLHL12 | 1:3~1:4 | Negative | Online Inquiry |
KLHL12 Gene Knockout Cell Lines are genetically engineered cell lines designed to facilitate the study of KLHL12 function through targeted gene knockout technology. The KLHL12 gene encodes a member of the kelch-like protein family, which is implicated in various cellular processes, including protein degradation and signal transduction pathways. By utilizing CRISPR/Cas9 technology for precise genomic editing, these cell lines provide a powerful tool for researchers aiming to dissect the biological roles of KLHL12 in various contexts, including cancer biology, neurodegenerative diseases, and cellular stress response mechanisms.
The functional mechanism behind KLHL12 knockout involves the introduction of double-strand breaks at the endogenous KLHL12 locus, leading to either insertions or deletions that ultimately disable gene expression. This knockout model is invaluable for elucidating the contributions of KLHL12 to cellular phenotypes and can aid in identifying novel therapeutic targets. In both research and clinical settings, understanding KLHL12’s role can provide insights into diseases driven by dysregulation of related pathways.
The scientific importance of KLHL12 Gene Knockout Cell Lines lies in their ability to facilitate high-throughput screening assays and functional studies, significantly advancing our understanding of protein interactions and regulatory mechanisms. Compared to alternatives such as siRNA-mediated knockdown, the permanent knockout effect of these cell lines allows for more stable and long-term studies.
For researchers and clinicians, these cell lines stand out due to their potential in revealing novel biomarkers and therapeutic targets, paving the way for breakthroughs in precision medicine. Moreover, the robust validation and quality assurance provided during the development of KLHL12 Gene Knockout Cell Lines ensure consistent performance and reliable results.
With a strong commitment to advancing biological research, our company leverages cutting-edge genomic editing technologies and deep expertise in cell line development, offering researchers the tools they need to push the boundaries of science and discover innovative solutions in healthcare.
Please note that all services are for research use only. Not intended for any clinical use.
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