Gene: SLC26A2
Official Full Name: solute carrier family 26 member 2provided by HGNC
Gene Summary: The diastrophic dysplasia sulfate transporter is a transmembrane glycoprotein implicated in the pathogenesis of several human chondrodysplasias. It apparently is critical in cartilage for sulfation of proteoglycans and matrix organization. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05475 | SLC26A2 Knockout cell line (HeLa) | Human | SLC26A2 | 1:3~1:6 | Negative | Online Inquiry |
KO05476 | SLC26A2 Knockout cell line (HCT 116) | Human | SLC26A2 | 1:2~1:4 | Negative | Online Inquiry |
KO05477 | SLC26A2 Knockout cell line (HEK293) | Human | SLC26A2 | 1:3~1:6 | Negative | Online Inquiry |
KO05478 | SLC26A2 Knockout cell line (A549) | Human | SLC26A2 | 1:3~1:4 | Negative | Online Inquiry |
SLC26A2 Gene Knockout Cell Lines are genetically engineered cellular models that have had the SLC26A2 gene disrupted or eliminated. This gene encodes for the solute carrier family 26 member 2 (SLC26A2), which plays a critical role in the transport of sulfate and other anions across cell membranes, influencing various biological functions such as cartilage development and maintenance. By specifically knocking out this gene, researchers gain valuable insights into its physiological roles and the consequences of its dysfunction.
The primary mechanism by which these cell lines function is through the absence of the SLC26A2 protein, allowing researchers to study downstream effects on cellular signaling pathways, ion transport, and metabolic processes. The resultant phenotypic changes, including disrupted sulfate transport, can closely mimic pathophysiological conditions associated with disorders such as skeletal dysplasia and multiple exostoses. This creates a powerful tool for investigating the biological and molecular mechanisms that underlie various diseases linked to SLC26A2 dysregulation.
The scientific importance of SLC26A2 Gene Knockout Cell Lines lies in their applicability in both fundamental research and translational medicine. They serve as an essential resource for investigating gene function, screening potential therapeutic compounds, and understanding the molecular basis of genetic diseases. In clinical settings, these cell lines can be instrumental in drug discovery, helping identify and validate novel therapeutic targets.
One of the significant advantages of utilizing SLC26A2 Gene Knockout Cell Lines over traditional research models is the specificity and precision of the gene knockout. Unlike other methods, such as pharmacological inhibition or transient transfection, these stable cell lines provide consistent and reproducible results, which are critical for high-throughput screening and experimental validation. Additionally, they cater to a wide range of experimental needs, from molecular biology analyses to biochemical assays.
For researchers and clinicians, the value of SLC26A2 Gene Knockout Cell Lines cannot be overstated. By harnessing these advanced cellular models, they can accelerate their research, enhance their understanding of related diseases, and ultimately translate their findings into innovative therapies. Our company prides itself on its vast expertise in genetic engineering and the development of high-quality biological products, ensuring that researchers have access to the most reliable and effective tools in their scientific pursuits.
Please note that all services are for research use only. Not intended for any clinical use.
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