Gene: LUC7L2
Official Full Name: LUC7 like 2, pre-mRNA splicing factorprovided by HGNC
Gene Summary: This gene encodes a protein that contains a C2H2-type zinc finger, coiled-coil region and arginine, serine-rich (RS) domain. A similar protein in mouse interacts with sodium channel modifier 1, and the encoded protein may be involved in the recognition of non-consensus splice donor sites in association with the U1 snRNP spliceosomal subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO22352 | LUC7L2 Knockout cell line (HeLa) | Human | LUC7L2 | 1:3~1:6 | Negative | Online Inquiry |
KO22353 | LUC7L2 Knockout cell line (HCT 116) | Human | LUC7L2 | 1:2~1:4 | Negative | Online Inquiry |
KO22354 | LUC7L2 Knockout cell line (HEK293) | Human | LUC7L2 | 1:3~1:6 | Negative | Online Inquiry |
KO22355 | LUC7L2 Knockout cell line (A549) | Human | LUC7L2 | 1:3~1:4 | Negative | Online Inquiry |
LUC7L2 Gene Knockout Cell Lines are genetically modified cell lines designed to eliminate the expression of the LUC7L2 gene, which plays a critical role in alternative splicing and RNA metabolism. These cell lines are indispensable tools for researchers seeking to study the functional consequences of LUC7L2 loss-of-function, aiding in the elucidation of its involvement in various biological processes and disease states.
The primary mechanism of action involves CRISPR/Cas9 technology, which enables precise gene editing. By introducing targeted double-strand breaks in the LUC7L2 gene, the cellular repair processes result in mutations that disrupt its expression. This knockout approach allows for detailed investigations into the resulting phenotypic changes, including alterations in cellular growth, differentiation, and response to external stimuli.
The scientific importance of LUC7L2 Gene Knockout Cell Lines is underscored by their application in fundamental research areas such as cancer biology, neurobiology, and developmental biology, where aberrations in splicing mechanisms have been linked to pathological conditions. Additionally, they provide a platform for testing therapeutic strategies aimed at correcting splicing defects, thus holding promise for translational applications.
Compared to alternative models, such as overexpression systems or whole-animal models, these cell lines offer a more controlled environment that enables high-throughput screening and detailed molecular assays without the confounding effects of a complete organism. This specificity leads to more reliable and reproducible results, essential for rigorous scientific inquiry.
For researchers and clinicians focused on RNA biology and its implications in health and disease, LUC7L2 Gene Knockout Cell Lines present a valuable asset, facilitating exploration into new therapeutic avenues. By leveraging our company’s expertise in advanced genetic engineering techniques and a deep understanding of RNA-related functions, we provide high-quality, validated cell lines that enhance research capabilities and drive scientific innovation.
Please note that all services are for research use only. Not intended for any clinical use.
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