Cat. No.: IBDAK-620527
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Sample Type | Cell culture extracts, Tissue Extracts |
Detection Method | Colorimetric |
Assay Type | Sandwich (quantitative) |
Assay Time | 1 h 30 min |
Assay Duration | One step assay |
Product Type | Redox Metabolism |
Sensitivity | 80.7 pg/ml |
Range | 234 pg/ml - 15000 pg/ml |
Species Reactivity | Reacts with: Mouse, Rat, Human |
Platform | Pre-coated microplate (12 x 8 well strips) |
Target
Function | Responds to activation by environmental stress and pro-inflammatory cytokines by phosphorylating a number of transcription factors, primarily components of AP-1 such as c-Jun and ATF2 and thus regulates AP-1 transcriptional activity. In T-cells, JNK1 and JNK2 are required for polarized differentiation of T-helper cells into Th1 cells.JNK2 isoforms display different binding patterns: alpha-1 and alpha-2 preferentially bind to c-Jun, whereas beta-1 and beta-2 bind to ATF2. However, there is no correlation between binding and phosphorylation, which is achieved at about the same efficiency by all isoforms. JUNB is not a substrate for JNK2 alpha-2, and JUND binds only weakly to it. |
Sequence Similarities | Belongs to the protein kinase superfamily. CMGC Ser/Thr protein kinase family. MAP kinase subfamily. Contains 1 protein kinase domain. |
Domain | The TXY motif contains the threonine and tyrosine residues whose phosphorylation activates the MAP kinases. |
Storage & Handling
Storage | Store at -20°C. Please refer to protocols. |