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SLC12A6 Knockout Cell Lines

Gene: SLC12A6

Official Full Name: solute carrier family 12 member 6provided by HGNC

Gene Summary: This gene is a member of the K-Cl cotransporter (KCC) family. K-Cl cotransporters are integral membrane proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The proteins encoded by this gene are activated by cell swelling induced by hypotonic conditions. Alternate splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are associated with agenesis of the corpus callosum with peripheral neuropathy. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO32414 SLC12A6 Knockout cell line (HeLa) Human SLC12A6 1:3~1:6 Negative Online Inquiry
KO32415 SLC12A6 Knockout cell line (HCT 116) Human SLC12A6 1:2~1:4 Negative Online Inquiry
KO32416 SLC12A6 Knockout cell line (HEK293) Human SLC12A6 1:3~1:6 Negative Online Inquiry
KO32417 SLC12A6 Knockout cell line (A549) Human SLC12A6 1:3~1:4 Negative Online Inquiry

Background

SLC12A6 Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the functionality of the SLC12A6 gene, which encodes a sodium-potassium-chloride co-transporter involved in ion homeostasis and cellular osmotic balance. These knockout cell lines serve as essential tools for researchers aiming to elucidate the biological roles of SLC12A6 in various physiological and pathological contexts. By creating these precise models, scientists can investigate the downstream effects of SLC12A6 depletion on cellular activities such as growth, apoptosis, and differentiation.

The key mechanism of action for SLC12A6 gene knockout involves CRISPR-Cas9 technology, which facilitates the targeted disruption of the gene. Researchers can effectively analyze how the absence of SLC12A6 influences ion transport dynamics, cellular responses to osmotic stress, and overall cellular function. Such mechanistic insights are invaluable, particularly in studies related to neurological disorders, renal functions, and other metabolic syndromes where ion transport plays a critical role.

The scientific importance of SLC12A6 knockout cell lines extends beyond basic research; they hold significant promise in clinical applications, including drug discovery and therapeutic testing. As it is implicated in conditions such as epilepsy and muscular dystrophies, understanding the effects of SLC12A6 disruption can lead to novel therapeutic strategies.

Compared to alternative models, SLC12A6 gene knockout cell lines offer enhanced specificity in studying the transporter’s functions without the confounding effects of other related transporters. Their establishment allows for repeated experimental use with consistent genetic backgrounds, providing reliable and reproducible results.

For researchers and clinicians, these cell lines represent an invaluable resource, driving innovation in both basic and applied biological research. Our company's expertise in creating high-fidelity genetic models ensures that you receive products with unparalleled accuracy and reliability, enabling you to push the boundaries of scientific discovery effectively.

Please note that all services are for research use only. Not intended for any clinical use.

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