mProX™ Human MAP2K3 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Expression of BCL2, BCL6, BCLXL, MAP2K3, MCL1, and MYC in DLBCL cell lines.
Oncogene expression in U-2946 and other DLBCL cell lines was evaluated using Western blot and qRT-PCR techniques.
Ref: Quentmeier, Hilmar, et al. "Diffuse large B cell lymphoma cell line U-2946: model for MCL1 inhibitor testing." PLoS One 11.12 (2016): e0167599.
Pubmed: 27907212
DOI: 10.1371/journal.pone.0167599
Research Highlights
miRNA-21 was found to have a reverse correlation with P38 MAPK activation following CVB3 infection. Furthermore, miRNA-21 overexpression was found to significantly inhibit the release of viral progeny and decrease the rate of myocyte apoptosis both in vitro and in vivo. These findings suggest that miRNA-21, by targeting the MAP2K3/P38 MAPK signaling, may be a potential therapeutic agent against CVB3 infection.
He, Feng, et al. "The protective role of microRNA-21 against coxsackievirus B3 infection through targeting the MAP2K3/P38 MAPK signaling pathway." Journal of translational medicine 17.1 (2019): 1-11.
Pubmed:
31585536
DOI:
10.1186/s12967-019-2077-y
According to these studies, a combination therapy of sevoflurane and propofol may prevent cardiac cells from being damaged during ischemia reperfusion (IR) by lowering the level of MAP2K3 and lowering cell apoptosis through the Bcl-2/Bax pathway.
Liu, Yanqin, et al. "Effect of combination therapy of propofol and sevoflurane on MAP2K3 level and myocardial apoptosis induced by ischemia-reperfusion in rats." International Journal of Clinical and Experimental Medicine 8.4 (2015): 6427.
Pubmed:
26131269