Gene: PLS3
Official Full Name: plastin 3provided by HGNC
Gene Summary: Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. Plastin 1 (otherwise known as Fimbrin) is a third distinct plastin isoform which is specifically expressed at high levels in the small intestine. The L isoform is expressed only in hemopoietic cell lineages, while the T isoform has been found in all other normal cells of solid tissues that have replicative potential (fibroblasts, endothelial cells, epithelial cells, melanocytes, etc.). The C-terminal 570 amino acids of the T-plastin and L-plastin proteins are 83% identical. It contains a potential calcium-binding site near the N terminus. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03555 | PLS3 Knockout cell line (HeLa) | Human | PLS3 | 1:3~1:6 | Negative | Online Inquiry |
KO03556 | PLS3 Knockout cell line (HCT 116) | Human | PLS3 | 1:2~1:4 | Negative | Online Inquiry |
KO03557 | PLS3 Knockout cell line (HEK293) | Human | PLS3 | 1:3~1:6 | Negative | Online Inquiry |
KO03558 | PLS3 Knockout cell line (A549) | Human | PLS3 | 1:3~1:4 | Negative | Online Inquiry |
PLS3 Gene Knockout Cell Lines are engineered cellular models designed to study the function of the PLS3 gene (plastin 3), which is implicated in various cellular processes, including cytoskeletal organization, cell motility, and intracellular signaling. These knockout models provide a valuable tool for researchers investigating the gene's role in health and disease, facilitating the analysis of its contributions to cellular dynamics and pathophysiological conditions.
The key function of the PLS3 Gene Knockout Cell Lines lies in the targeted disruption of the PLS3 gene, effectively eliminating its expression. This genetic modification enables researchers to observe the resultant phenotypic changes in cell behavior, allowing for insights into the gene's contributions to cellular functions. The mechanisms of action observed in these knockout cell lines often include alterations in actin filament dynamics and cellular adhesion properties, thereby providing critical information on how loss-of-function mutations in PLS3 can contribute to diseases such as neuromuscular disorders and cancer.
The scientific importance of PLS3 Gene Knockout Cell Lines is underscored by their applications in both basic research and clinical settings. Researchers can leverage these models to elucidate the roles of PLS3 in disease mechanisms, potentially leading to the identification of new therapeutic targets. Additionally, these cell lines can be instrumental in drug screening initiatives, testing the efficacy of new treatments aimed at modulating PLS3-related pathways.
What sets PLS3 Gene Knockout Cell Lines apart from alternatives is their specificity and rigor in gene editing, accomplished through advanced CRISPR/Cas9 technology. This ensures a precise disruption of the PLS3 gene without off-target effects, offering researchers high confidence in their experimental outcomes. Furthermore, the availability of multiple knockout clones allows for comparative studies within the same experimental framework, enhancing reproducibility and reliability.
In summary, PLS3 Gene Knockout Cell Lines represent an invaluable resource for researchers and clinicians dedicated to understanding the complexities of gene function and disease. By integrating this tool into their research, users can advance our knowledge of PLS3's role in health and disease, paving the way for innovative therapeutic strategies. Our company prides itself on its commitment to facilitating groundbreaking research through high-quality biological products, ensuring that researchers have access to the latest advancements in genetic engineering.
Please note that all services are for research use only. Not intended for any clinical use.
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