Gene: LXN
Official Full Name: latexinprovided by HGNC
Gene Summary: This gene encodes the only known protein inhibitor of zinc-dependent metallocarboxypeptidases. The encoded protein, latexin, downregulates the population size of hematopoietic stem cells. This protein is found to be downregulated in cancer cells because of promoter hypermethylation. [provided by RefSeq, Jul 2020]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO16417 | LXN Knockout cell line (HeLa) | Human | LXN | 1:3~1:6 | Negative | Online Inquiry |
KO16418 | LXN Knockout cell line (HEK293) | Human | LXN | 1:3~1:6 | Negative | Online Inquiry |
KO16419 | LXN Knockout cell line (A549) | Human | LXN | 1:3~1:4 | Negative | Online Inquiry |
LXN Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to silenced the expression of the LXN gene, providing researchers with invaluable tools for studying gene function, cellular pathways, and disease mechanisms. The creation of these knockout cell lines utilizes advanced CRISPR-Cas9 technology, which allows for precise editing of the genome, leading to the targeted removal of the LXN gene. By observing the phenotypic and functional changes that occur in the absence of LXN, scientists can gain insights into its role in various biological processes, including metabolism, development, and pathogenesis.
These cell lines exhibit critical functions in elucidating the molecular underpinnings of diseases such as cancer and metabolic disorders, where the LXN gene has been implicated. Their use within research settings facilitates a better understanding of gene interactions and can pave the way for novel therapeutic strategies. In clinical applications, the insights derived from experimenting with these knockout lines hold promise for developing targeted treatments that can mitigate the impact of LXN-related pathologies.
LXN Gene Knockout Cell Lines offer several distinct advantages over traditional methods of gene silencing, such as siRNA treatments, including stable gene disruption that allows for long-term studies and reproducibility in experiments. Additionally, the CRISPR-Cas9 technology ensures a complete and specific knockout of the LXN gene, minimizing off-target effects and enhancing the validity of experimental outcomes.
Researchers and clinicians seeking to explore gene function with precision will find LXN Gene Knockout Cell Lines to be invaluable assets in their investigation of intricate biological networks. These tools not only enable cutting-edge research but also contribute to the progressive understanding of complex diseases, ultimately leading toward more effective therapeutic interventions.
With a commitment to excellence in genetic engineering and a deep understanding of molecular biology, our company is proud to offer this state-of-the-art product, empowering scientists globally to advance their research and improve clinical therapies.
Please note that all services are for research use only. Not intended for any clinical use.
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