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Involved in nonsense-mediated mRNA decay (NMD) by acting as a bridge between the mRNA decapping complex and the NMD machinery. 再加上，我们可以发PNRC2 蛋白 (10) 和 和数多这个蛋白质的别的产品。
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Rat (Rattus) Polyclonal PNRC2 Primary Antibody for WB - ABIN4893631
Graber, Freemantle, Anadolu, Hébert-Seropian, MacAdam, Shin, Hoang, Alain, Lacaille, Sossin: UPF1 Governs Synaptic Plasticity through Association with a STAU2 RNA Granule. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2017
UPF1 (显示 UPF1 抗体) interacts with PNRC2 and that it triggers 5'-3' exonucleolytic decay of reporter transcripts in tethering assays. PNRC2 is probably an important mRNA decapping factor but that it does not appear to be required for nonsense-mediated mRNA decay.
GR and PNRC2 interact in a ligand-dependent manner to recruit UPF1 (显示 UPF1 抗体) for rapid mRNA degradation
PNRC2 acts in synergy with Dcp1a (显示 DCP1A 抗体) to stimulate the decapping activity of Dcp2 (显示 DCP2 抗体) by bridging the interaction between Dcp1a (显示 DCP1A 抗体) and Dcp2 (显示 DCP2 抗体).
Not only PNRC2 but also the corepressor TLE1 (显示 TLE1 抗体) functioned as ERRgamma (显示 ESRRG 抗体) coactivator in a reporter gene analysis.
PNRC2 plays an essential role in mammalian Nonsense-mediated mRNA decay (NMD), mediating the interaction between the NMD machinery and the decapping complex.
The finding that the PNRC2 promoter is activated by NFY and repressed by E2F1 (显示 E2F1 抗体) indicates that in addition to functioning as nuclear receptor coactivator, PNRC2 may also play a role in the cell cycle.
Study provides evidence that PNRC2 plays one or more important roles in controlling the energy balance between energy storage and energy expenditure. PNRC2 may be a new target in the treatment of obesity and related metabolic diseases.
Pnrc2 promotes 3'UTR (显示 UTS2R 抗体)-mediated decay of developmentally-regulated segmentation clock transcripts.
Involved in nonsense-mediated mRNA decay (NMD) by acting as a bridge between the mRNA decapping complex and the NMD machinery. May act by targeting the NMD machinery to the P-body and recruiting the decapping machinery to aberrant mRNAs. Required for upf1/rent1 localization to the P-body. Also acts as a nuclear receptor coactivator (By similarity).