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- 2025年07月13日
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100
- 供应商：
艾美捷科技
- 英文名：
AP-1 Reporter - HEK293 Recombinant Cell Line (JNK signaling pathway)
AP-1 报告基因 - HEK293 重组细胞系（JNK 信号通路），AP-1 Reporter - HEK293 Recombinant Cell Line (JNK signaling pathway) ，AP-1 报告基因 - HEK293 重组细胞系（JNK 信号通路）,AP-1 Reporter - HEK293 Recombinant Cell Line (JNK signaling pathway)
AP-1 报告基因 - HEK293 重组细胞系（JNK 信号通路）-AP-1 Reporter - HEK293 Recombinant Cell Line (JNK signaling pathway)
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应激激活蛋白激酶/c-junn末端激酶(SAPK/JNK)家族包括应激激活的丝裂原活化蛋白激酶(MAPKs)、炎性细胞因子、丝裂原、癌基因以及细胞分化和形态发生诱导剂。在激活SAPK/JNK途径后，MAP激酶激酶磷酸化并激活JNKs。激活的JNKs易位到细胞核，在那里它们磷酸化并激活转录因子如c-Jun。然后cJun与激活蛋白-1(AP1)应答元件结合并诱导ap1转录。
监测JNK信号通路活性和ap1介导的活性。•筛选JNK信号传导途径的激活剂或抑制剂。
AP-1 报告基因 - HEK293 重组细胞系（JNK 信号通路）-AP-1 Reporter - HEK293 Recombinant Cell Line (JNK signaling pathway) 收到后立即储存在液氮中。
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文献和实验Structural analog of Cyclotheonellazole A, and synthetic method therefor and application method thereof.
Therapeutic Potential of Dimethyl Fumarate for the Treatment of High-Fat/High-Sucrose Diet-Induced Obesity.
Inhibitors of malaria parasite cyclic nucleotide phosphodiesterases block asexual blood-stage development and mosquito transmission
Using Reporter Gene Technologies to Detect Changes in cAMP as a Result of GPCR Activation
). This chapter provides a generic protocol for the successful execution of a reporter gene assay for GPCRs, stably transfected within Chinese hamster ovary cell lines, signaling through the Gs pathway. It also highlights areas to investigate when developing
embryonic stem (ES) cells. Recessive genetic screens are feasible in ES cells that are Bloom-syndrome protein (Blm-) deficient. Therefore, we constructed a reporter cell line in Blm-deficient ES cells to isolate RNAi mutants through a simple drug-selection
Cell-Based Assays for Identification of Aryl Hydrocarbon Receptor (AhR) Activators
and its signaling pathway in endogenous physiological functions and its involvement in immune cell development and human diseases has made it a target for development of therapeutic agents. The ability of the AhR to stimulate gene expression in a ligand-specific
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