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[供應]hkb-koalpk——Knockout ALPK1 HEK 293 reporter cells

貨物所在地:北京北京市

更新時間:2025-04-09 09:30:35

有效期:2025年4月9日 -- 2026年4月10日

已獲點擊:43

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HEK-Blue™ KO-ALPK1 cells were generated from HEK-Blue™ Null1-v cells through the stable knockout of the ALPK1 gene.

Cell Line Stability 

Cells will undergo genotypic changes over time resulting in reduced responsiveness in normal cell culture conditions. Genetic instability is a biological phenomenon that occurs in all stably transfected cells. Therefore, it is critical to prepare an adequate number of frozen stocks at early passages. HEK-Blue™ KO-ALPK1 cells should not be passaged more than 20 times to remain fully functional.

HEK-Blue™ KO-ALPK1 cells were generated from HEK-Blue™ Null1-v cells through the stable knockout of the ALPK1 gene. The parental cells derive from human embryonic kidney 293 (HEK-293) cells. HEK-Blue™ KO-ALPK1 cells express a secreted embryonic alkaline phosphatase (SEAP) under the control of an NF-κB inducible promoter comprised of an IFN-β minimal promoter fused to five NF-κB and AP-1 binding sites. Levels of SEAP in the supernatant can be easily determined with HEK-Blue™ Detection, a SEAP detection cell culture medium. Unlike their parental cell line, HEK?Blue™ KO-ALPK1 cells do not respond to cytosolic ADP-Heptose. However, they do respond to other NF-κB inducers such as TNF-α and IL-1β. HEK?Blue™ KO-ALPK1 cells are resistant to Zeocin™


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