Gene: SLC12A1
Official Full Name: solute carrier family 12 member 1provided by HGNC
Gene Summary: This gene encodes a kidney-specific sodium-potassium-chloride cotransporter that is expressed on the luminal membrane of renal epithelial cells of the thick ascending limb of Henle's loop and the macula densa. It plays a key role in concentrating urine and accounts for most of the NaCl resorption. It is sensitive to such diuretics as furosemide and bumetanide. Some Bartter-like syndromes result from defects in this gene. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their biological validity in humans has not been experimentally proven.[provided by RefSeq, May 2010]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA13649 | SLC12A1 Knockout cell line (AC16) | Human | SLC12A1 | 1:3-1:4 | negative | Online Inquiry |
| KOA29089 | SLC12A1 Knockout cell line (BEAS-2B) | Human | SLC12A1 | 1:3~1:4 | negative | Online Inquiry |
| KOA44526 | SLC12A1 Knockout cell line (U-2932) | Human | SLC12A1 | 1:2-1:4 | negative | Online Inquiry |
| KOA59903 | SLC12A1 Knockout cell line (TPC-1) | Human | SLC12A1 | 1:5-1:8 | negative | Online Inquiry |
| KOA75328 | SLC12A1 Knockout cell line (NCM460) | Human | SLC12A1 | 1:2~1:3 | negative | Online Inquiry |
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