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GPS2 encodes a protein involved in G protein-mitogen-activated protein kinase (MAPK) signaling cascades. Additionally we are shipping GPS2 Proteins (4) and many more products for this protein.
Showing 10 out of 72 products:
Human Monoclonal GPS2 Primary Antibody for EIA, WB - ABIN317522
Peng, Breiding, Sverdrup, Richard, Androphy: AMF-1/Gps2 binds p300 and enhances its interaction with papillomavirus E2 proteins. in Journal of virology 2000
Show all 2 references for ABIN317522
Human Monoclonal GPS2 Primary Antibody for ELISA, WB - ABIN561119
Sanyal, Båvner, Haroniti, Nilsson, Lundåsen, Rehnmark, Witt, Einarsson, Talianidis, Gustafsson, Treuter: Involvement of corepressor complex subunit GPS2 in transcriptional pathways governing human bile acid biosynthesis. in Proceedings of the National Academy of Sciences of the United States of America 2007
our studies identify GPS2 functions as a tumor suppressor in LPS (show IRF6 Antibodies) and its downregulation is correlated to prognosis of LPS (show IRF6 Antibodies).
Posttranslational modification of GPS2 by SUMOylation may serve as a key factor that regulates the function of GPS2 in vivo.
regulation of GPS2 by posttranslational modifications provides an effective strategy for modulating its molecular function within the nuclear compartment.
Chromosomal translocation in a pediatric undifferentiated spindle cell sarcoma have characterized this alteration to show rearrangement of the MLL4 (show MLL2 Antibodies) and GPS2 genes, resulting in fusion gene MLL4 (show MLL2 Antibodies)-GPS2, the expression of which promotes independent growth.
GPS2 is required for the association of viral NS5A with VAP-A (show VAPA Antibodies) and hepatitis C virus replication.
expression of the transcriptional corepressor complex subunits GPS2 and SMRT (show NCOR2 Antibodies) was significantly reduced in obese adipose tissue, inversely correlated to inflammatory status
Results show for the first time that GPS-2 is differentially methylated at a site that lacks known methylation motifs and that the methylation state is detected by the immune system
metabolically important coregulator GPS2 functions as a hitherto unrecognized transrepression mediator of interactions between SUMOylated nuclear receptors and the N-CoR (show NCOR1 Antibodies) corepressor complex
Results show that the N-CoR (show NCOR1 Antibodies)-HDAC3 (show HDAC3 Antibodies) complex inhibits JNK (show MAPK8 Antibodies) activation through the associated GPS2 subunit and thus could potentially provide an alternative mechanism for hormone-mediated antagonism of AP-1 (show FOSB Antibodies) function.
the GPS2 might function in concert with hMSH4 (show MSH4 Antibodies)-hMSH5 (show MSH5 Antibodies) during the process of homologous recombination.
GPS2 is required for restricting the activation of TLR and BCR (show BCR Antibodies) signaling pathways and the AKT (show AKT1 Antibodies)/FOXO1 (show FOXO1 Antibodies) pathway in immune cells based on direct inhibition of Ubc13 (show UBE2N Antibodies) enzymatic activity
GPS2 stabilizes KDM4A (show KDM4A Antibodies) on target promoters by inhibiting Ubc13 (show UBE2N Antibodies)/RNF8 (show RNF8 Antibodies) ubiquitination.
GPS2 binds to active PPARgamma (show PPARG Antibodies), facilitates its repression by NCoR (show NCOR1 Antibodies), and is required for the optimal NCoR (show NCOR1 Antibodies) corepressor function for PPARgamma (show PPARG Antibodies).
GPS2 as a molecular guardian required for precise control of inflammatory responses involved in immunity and homeostasis.
This gene encodes a protein involved in G protein-mitogen-activated protein kinase (MAPK) signaling cascades. When overexpressed in mammalian cells, this gene could potently suppress a RAS- and MAPK-mediated signal and interfere with JNK activity, suggesting that the function of this gene may be signal repression. The encoded protein is an integral subunit of the NCOR1-HDAC3 (nuclear receptor corepressor 1-histone deacetylase 3) complex, and it was shown that the complex inhibits JNK activation through this subunit and thus could potentially provide an alternative mechanism for hormone-mediated antagonism of AP1 (activator protein 1) function.
G protein pathway suppressor 2
, G-protein pathway suppressor 2