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Cat.No.: F9786
| Dilution |
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|
| Application |
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| WB |
| Reactivity |
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| Human, Mouse, Rat, Monkey |
| Source |
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| Rabbit Monoclonal Antibody |
| Storage Buffer |
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| PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3 |
| Storage (from the date of receipt) |
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| -20°C (avoid freeze-thaw cycles), 2 years |
| Predicted MW |
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| 24 kDa |
| Specificity |
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| Phospho-MOB1 (Thr12) Antibody [F15P10] detects endogenous levels of total MOB1 protein only when it is phosphorylated at Thr12. |
| Clone |
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| F15P10 |
| Synonym(s) |
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| MOB kinase activator 1A; Mob1α; MOBKL1A; MOB1A |
| Background |
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| Phospho-MOB1 (Thr12) designates the activated conformation of MOB1A/B adaptor proteins central to the Hippo tumor suppressor pathway that governs organ size, proliferation, and apoptosis through kinase cascade amplification. MOB1 organizes a compact globular fold with an N-terminal extension and core domain that undergoes phosphorylation at Thr12 by MST1/2 kinases, stabilizing an open conformation where the Switch helix dissociates to expose binding interfaces for LATS1/2 N-terminal regulatory regions. This phospho-Thr12 event allosterically activates LATS1/2 catalytic domains through dynamic scaffolding that juxtaposes MST-phosphorylated activation loops with MOB1 phospho-sites, enabling trans-phosphorylation that ramps up YAP/TAZ inhibitory serine phosphorylation for cytoplasmic retention and proteasomal degradation via β-TRCP ubiquitin ligase. Phospho-MOB1 further engages NDR1/2 kinases with differential affinity modulated by Thr12/Thr35 phosphates that pull N-terminal strands into β-sheet configurations stabilizing kinase-MOB complexes for mitotic exit and ploidy control. The resultant LATS-YAP/TAZ axis integrates upstream inputs, such as cell density and mechanotransduction, through Merlin-expanded sensing to transcriptionally repress CTGF, Cyr61, and c-Myc, thereby facilitating contact inhibition during epithelial morphogenesis. Phospho-MOB1 coordinates tissue homeostasis in liver regeneration and neural tube closure, with ubiquitous expression ensuring robust pathway fidelity across proliferative niches. |
| References |
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