SLC12A3 Stable Expression Cell Line (293T)
This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene.
本产品仅供进一步科研使用,不得用于诊断、治疗、临床及其他用途。
EZ-iScreen™产品优势
该类细胞株稳定表达Cas9蛋白,仅需转染gRNA,即可实现基因敲除,而同时转染gRNA和供体DNA,则可实现基因敲入/点突变。
在该类细胞的基础上已成功构建大量基因敲除细胞株,且基因敲除效率均提高5-10倍。
该类细胞株经过优化,代次低、活性高、状态好,适用于各类基因编辑实验。
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