Gene: SLC12A7
Official Full Name: solute carrier family 12 member 7provided by HGNC
Gene Summary: Enables protein kinase binding activity. Predicted to be involved in several processes, including chloride ion homeostasis; monoatomic ion transmembrane transport; and potassium ion homeostasis. Part of protein-containing complex. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO31592 | SLC12A7 Knockout cell line (HeLa) | Human | SLC12A7 | 1:3~1:6 | Negative | Online Inquiry |
KO31593 | SLC12A7 Knockout cell line (HCT 116) | Human | SLC12A7 | 1:2~1:4 | Negative | Online Inquiry |
KO31594 | SLC12A7 Knockout cell line (HEK293) | Human | SLC12A7 | 1:3~1:6 | Negative | Online Inquiry |
KO31595 | SLC12A7 Knockout cell line (A549) | Human | SLC12A7 | 1:3~1:4 | Negative | Online Inquiry |
SLC12A7 Gene Knockout Cell Lines represent a cutting-edge biotechnological tool designed for the study of cellular ion transport mechanisms and their implications in various physiological and pathological processes. This product consists of genetically engineered cell lines where the SLC12A7 gene, encoding the sodium-potassium-chloride cotransporter 1 (NKCC1), has been intentionally knocked out. Utilizing CRISPR-Cas9 technology, these cell lines allow researchers to dissect the role of SLC12A7 in ion homeostasis, cell volume regulation, and osmotic balance, providing an invaluable model for understanding diseases where dysregulation of these processes is implicated, such as hypertension, heart failure, and certain genetic disorders.
Key functions of the SLC12A7 deletion include altered intracellular ion concentrations, which can serve as a basis for investigating downstream signaling pathways and cellular responses under varying physiological conditions. The perturbation induced by the knockout facilitates the exploration of how changes in ionic balance affect cellular functions such as proliferation, apoptosis, and differentiation, thereby providing critical insights into cell biology and disease mechanisms.
From a scientific perspective, these knockout cell lines can enhance research capabilities in pharmacology, toxicology, and developmental biology by enabling the identification of specific ion transport inhibitors, potential drug targets, and gene therapies. This can lead to advancements in clinical settings, particularly in the development of innovative treatments for ion transport-related disorders.
Compared to alternatives, the SLC12A7 Gene Knockout Cell Lines stand out due to their precise genetic modification, high integrity, and reproducibility, allowing for reliable and consistent experimental results. Additionally, these cell lines can be easily incorporated into high-throughput screening platforms, thereby accelerating research timelines and outcomes.
The value of this product to researchers and clinicians lies in its ability to provide a deeper understanding of the SLC12A7 gene’s contribution to human health and disease, driving forward innovative research and therapeutic strategies. Our company is dedicated to delivering high-quality biological products, backed by years of expertise in genetic engineering and cell line development, ensuring that our SLC12A7 Gene Knockout Cell Lines meet the highest standards for research excellence.
Please note that all services are for research use only. Not intended for any clinical use.
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