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DDX6 Antibody, A300-460A

Rabbit anti-DDX6 Antibody, Affinity Purified

Human, Mouse
WB, IP, IHC-P, IF
Rabbit
Polyclonal
Unconjugated
Whole IgG

Citations (33)

Sundararaman B et al. Resources for the Comprehensive Discovery of Functional RNA Elements. Mol Cell. 2016;61(6):903-13.
Applications: ICC, RIP, WB
Tsalikis J et al. Intracellular Bacterial Pathogens Trigger the Formation of U Small Nuclear RNA Bodies (U Bodies) through Metabolic Stress Induction. J Biol Chem. 2015;290(34):20904-18.
Kamenska A et al. Human 4E-T represses translation of bound mRNAs and enhances microRNA-mediated silencing. Nucleic Acids Res. 2014;42(5):3298-313.
Yasuda-inoue M et al. DDX3 RNA helicase is required for HIV-1 Tat function. Biochem Biophys Res Commun. 2013;441(3):607-11.
Huys A et al. Modulation of hepatitis C virus RNA accumulation and translation by DDX6 and miR-122 are mediated by separate mechanisms. PLoS ONE. 2013;8(6):e67437.
Applications: WB
Yasuda-inoue M et al. Distinct DDX DEAD-box RNA helicases cooperate to modulate the HIV-1 Rev function. Biochem Biophys Res Commun. 2013;434(4):803-8.
Pager CT et al. Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules. Virology. 2013;435(2):472-84.
Applications: WB
Chahar HS et al. P-body components LSM1, GW182, DDX3, DDX6 and XRN1 are recruited to WNV replication sites and positively regulate viral replication. Virology. 2013;436(1):1-7.
Applications: ICC
Novotny I et al. Nuclear LSm8 affects number of cytoplasmic P-bodies via controlling cellular distribution of LSm proteins. Mol Biol Cell. 2012 Oct;23(19):3776-85.
Applications: ICC
Ernoult-Lange M et al. Multiple binding of repressed mRNAs by the P-body protein Rck/p54. RNA. 2012 Sep;18(9):1702-15.
Crist CG et al. Muscle satellite cells are primed for myogenesis but maintain quiescence with sequestration of Myf5 mRNA targeted by microRNA-31 in mRNP granules. Cell Stem Cell. 2012 Jul 6;11(1):118-26.
Cougot N et al. The Dual Organization of P-bodies Revealed by Immunoelectron Microscopy and Electron Tomography. J Mol Biol. 2012 Jun 29;420(1-2):17-28.
Applications: ICC
Marnef A et al. RNA-related nuclear functions of human Pat1b, the P-body mRNA decay factor. Mol Biol Cell. 2012 Jan;23(1):213-24.
Applications: ICC
Ariumi Y et al. Hepatitis C virus hijacks P-body and stress granule components around lipid droplets. J Virol. 2011 Jul;85(14):6882-92.
Applications: ICC, WB
Saito K et al. MicroRNA 130 family regulates the hypoxia response signal through the P-body protein DDX6. Nucleic Acids Res. 2011 Aug;39(14):6086-99.
Applications: ICC, WB
Totaro A et al. The human Pat1b protein: a novel mRNA deadenylation factor identified by a new immunoprecipitation technique. Nucleic Acids Res. 2011 Jan;39(2):635-47.
Applications: WB
Marnef A et al. Distinct functions of maternal and somatic Pat1 protein paralogs. RNA. 2010 Nov;16(11):2094-107.
Applications: ICC, WB
Jangra RK et al. DDX6 (Rck/p54) is required for efficient hepatitis C virus replication but not for internal ribosome entry site-directed translation. J Virol. 2010 Jul;84(13):6810-24.
Applications: ICC, WB
Kemler I et al. Live-cell coimaging of the genomic RNAs and Gag proteins of two lentiviruses. J Virol. 2010 Jul;84(13):6352-66.
Applications: ICC
Savas JN et al. A role for huntington disease protein in dendritic RNA granules. J Biol Chem. 2010 Apr 23;285(17):13142-53.
Applications: ICC
Emara MM et al. Angiogenin-induced tRNA-derived stress-induced RNAs promote stress-induced stress granule assembly. J Biol Chem. 2010 Apr 2;285(14):10959-68.
Applications: ICC
Souquere S et al. Unravelling the ultrastructure of stress granules and associated P-bodies in human cells. J Cell Sci. 2009 Oct 15;122(Pt 20):3619-26.
Applications: ICC
Taddeo B et al. The virion-packaged endoribonuclease of herpes simplex virus 1 cleaves mRNA in polyribosomes. Proc Natl Acad Sci U S A. 2009 Jul 21;106(29):12139-44.
Applications: ICC
Otsuka Y et al. Identification of a cytoplasmic complex that adds a cap onto 5'-monophosphate RNA. Mol Cell Biol. 2009 Apr;29(8):2155-67.
Applications: ICC
Cougot N et al. Dendrites of mammalian neurons contain specialized P-body-like structures that respond to neuronal activation. J Neurosci. 2008 Dec 17;28(51):13793-804.
Applications: ICC
Zhai Y et al. Coordinated changes in mRNA turnover, translation, and RNA processing bodies in bronchial epithelial cells following inflammatory stimulation. Mol Cell Biol. 2008 Dec;28(24):7414-26.
Applications: WB
Ernoult-Lange M et al. Nucleocytoplasmic traffic of CPEB1 and accumulation in Crm1 nucleolar bodies. Mol Biol Cell. 2009 Jan;20(1):176-87.
Applications: ICC
Zheng D et al. Deadenylation is prerequisite for P-body formation and mRNA decay in mammalian cells. J Cell Biol. 2008 Jul 14;182(1):89-101.
Applications: WB
Morris AR et al. Ribonomic analysis of human Pum1 reveals cis-trans conservation across species despite evolution of diverse mRNA target sets. Mol Cell Biol. 2008 Jun;28(12):4093-103.
Applications: ICC
Marin M et al. Human immunodeficiency virus type 1 Vif functionally interacts with diverse APOBEC3 cytidine deaminases and moves with them between cytoplasmic sites of mRNA metabolism. J Virol. 2008 Jan;82(2):987-98.
Applications: ICC
Song MG et al. 3' Terminal oligo U-tract-mediated stimulation of decapping. RNA. 2007 Dec;13(12):2356-65.
Applications: WB
Chu CY et al. Translation repression in human cells by microRNA-induced gene silencing requires RCK/p54. PLoS Biol. 2006 Jul;4(7):e210.
Applications: WB
Wichroski MJ et al. Human retroviral host restriction factors APOBEC3G and APOBEC3F localize to mRNA processing bodies. PLoS Pathog. 2006 May;2(5):e41.
Applications: WB