Use your antibodies-online credentials, if available.
Il n’y a pas de produits dans votre liste de comparaison.
Votre panier est vide.
Afficher toutes les espèces
Afficher tous les synonymes
Sélectionnez vos espèces et l'application
anti-Human FMR1 Anticorps:
anti-Rat (Rattus) FMR1 Anticorps:
anti-Mouse (Murine) FMR1 Anticorps:
Vous arrivez à notre recherche pré-filtrée.
Fruit Fly (Drosophila melanogaster) Monoclonal FMR1 Primary Antibody pour ICC, IF - ABIN108598
Wan, Dockendorff, Jongens, Dreyfuss: Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein. dans Molecular and cellular biology 2000
Show all 7 Pubmed References
Fruit Fly (Drosophila melanogaster) Monoclonal FMR1 Primary Antibody pour ICC, IF - ABIN108599
Callan, Clements, Ahrendt, Zarnescu: Fragile X Protein is required for inhibition of insulin signaling and regulates glial-dependent neuroblast reactivation in the developing brain. dans Brain research 2012
Show all 7 Pubmed References
Bat Polyclonal FMR1 Primary Antibody pour WB - ABIN610747
Anderson, Teutsch, Dong, Wortis: An essential role for Bruton's [corrected] tyrosine kinase in the regulation of B-cell apoptosis. dans Proceedings of the National Academy of Sciences of the United States of America 1996
Show all 2 Pubmed References
Human Monoclonal FMR1 Primary Antibody pour ELISA, WB - ABIN515777
Schutzius, Bleckmann, Kapps-Fouthier, di Giorgio, Gerhartz, Weiss: A quantitative homogeneous assay for fragile X mental retardation 1 protein. dans Journal of neurodevelopmental disorders 2013
Human Polyclonal FMR1 Primary Antibody pour ELISA, WB - ABIN560935
Tucker, Richards, Lardelli: Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome. dans Human molecular genetics 2006
Chlamydomonas reinhardtii (C. reinhardtii) Polyclonal FMR1 Primary Antibody pour WB - ABIN1720852
Subramanian, Dubini, Astling, Laurens, Old, Grossman, Posewitz, Seibert: Profiling Chlamydomonas metabolism under dark, anoxic H2-producing conditions using a combined proteomic, transcriptomic, and metabolomic approach. dans Journal of proteome research 2014
Human Polyclonal FMR1 Primary Antibody pour ELISA, IHC (p) - ABIN451678
Hanson, Blank, Valenzuela, Garner, Madison: The functional nature of synaptic circuitry is altered in area CA3 of the hippocampus in a mouse model of Down's syndrome. dans The Journal of physiology 2007
Human Monoclonal FMR1 Primary Antibody pour IF, IHC - ABIN966157
Dobson, Kube, Timmerman, Krushel: Identifying intrinsic and extrinsic determinants that regulate internal initiation of translation mediated by the FMR1 5' leader. dans BMC molecular biology 2008
Human Polyclonal FMR1 Primary Antibody pour FACS, IHC (p) - ABIN390866
Yuhas, Walichiewicz, Pan, Zhang, Casillas, Hagerman, Tassone: High-risk fragile x screening in Guatemala: use of a new blood spot polymerase chain reaction technique. dans Genetic testing and molecular biomarkers 2009
Show all 2 Pubmed References
Human Polyclonal FMR1 Primary Antibody pour ELISA, WB - ABIN4312232
Dölen, Osterweil, Rao, Smith, Auerbach, Chattarji, Bear: Correction of fragile X syndrome in mice. dans Neuron 2007
Stored oocytes lacking FMR1 usually generate embryos with severe neural defects, unlike stored wild-type oocytes, which suggests that translation of multiple large proteins by stored mRNAs is defective in fragile X syndrome and possibly other autism spectrum disorders.
This FMRP activity is mediated solely via a second conserved RNA-binding protein, LIN-28 (Montrer LIN28A Anticorps), known to boost insulin (Montrer INS Anticorps) signaling in stem cells. Via LIN-28 (Montrer LIN28A Anticorps), FMRP controls progenitor cell behavior by post-transcriptionally repressing the level of insulin receptor (InR (Montrer INSR Anticorps)).
DTor and DFMRP immunoreactivities were partially colocalized in several cellular organelles in larval muscles
Fmr1 protein associates with ninaE (Montrer RHO Anticorps) mRNA and represses its translation.
Our data strongly support a gain-of-function pathogenic mechanism of PQBP1 (Montrer PQBP1 Anticorps) c.459_462delAGAG and c.463_464dupAG mutations, and suggest that therapeutic strategies to restore FMRP function may be beneficial for those patients
dFMRP cooperates with Piwi in maintaining genome integrity by silencing heterochromatic genes and suppressing transposon expression.
results show Fragile X Mental Retardation Protein (FMRP) shapes neuron class-specific calcium signaling in excitatory vs. inhibitory neurons in developing learning/memory circuitry, and that FMRP mediates activity-dependent regulation of calcium signaling specifically during the early-use critical period.
results support a model whereby dFMRP can modulate the neurotoxicity caused by TDP-43 (Montrer TARDBP Anticorps) overexpression
demonstrate that Zfrp8 genetically interacts with Fmr1 and tral (Montrer LSM14A Anticorps) in an antagonistic manner. Zfrp8 and FMRP both control heterochromatin packaging, also in opposite ways
dFmr1 protein is essential for proper cardiac function and establish the fly as a new model for studying the role(s) of FraX proteins in the heart.
Study found no significant relationship between the longitudinal changes of the CGG repeat in the FMR1 promoter region and premature ovarian failure etiology which can be attributed to the genetic heterogeneity nature of the disease, the possible involvement of the other genomic variations with the ovarian function and the reproductive health.
Agenet domain of FMRP binds FUS (Montrer FUS Anticorps).
Our male patient had a pattern of the FMR1 size mosaic with both premutation (129 CGG) and full mutation (over 200) fragments
AKT (Montrer AKT1 Anticorps) inhibition led to decreased FMRP levels, as expected due to the known FMR1/FMRP negative feedback loop. But rFSH and the mTOR (Montrer FRAP1 Anticorps) inhibition increased them, indicating a decoupling of this FMR1/FMRP negative feedback loop in our model system
The CGG expanded allele of the FMR1 gene might be associated with unexplained multiple miscarriages.
Fragile X-associated disorders encompass several conditions, which are caused by expansion mutations in the fragile X mental retardation 1 (FMR1) gene.
We demonstrate that romidepsin, an inhibitor of class I histone deacetylases, does not activate FMR1 expression in patient cell cultures, whereas vorinostat, an inhibitor of classes I and II histone deacetylases, activates a low level of FMR1 expression in some patient cell lines
the current study shows lower rates of blastocyst development per metaphase II oocyte and 2PN embryos in FMR1 pre-mutation carriers compared to age-matched controls.
Next-generation sequencing in human melanoma cells revealed that FMRP regulates a large number of mRNAs involved in relevant processes of melanoma progression
The naturally occurring Fragile XFMR1 5' region undergoes inactivation post implantation in a Dicer (Montrer DICER1 Anticorps)/Ago-dependent targeted process which involves local SUV39H (Montrer SUV39H1 Anticorps)-mediated tri (Montrer VANGL2 Anticorps)-methylation of histone H3K9. Fragile X syndrome may come about through inadvertent siRNA-mediated heterochromatinization.
We identified thousands of clustered RNA editing sites in the zebrafish transcriptome and showed that Fmrp biochemically interacts with the Adar2a protein. The expression levels of the adar (Montrer ADAR Anticorps) genes and Adar2 (Montrer ADARB1 Anticorps) protein increased in fmr1-/- zebrafish
Loss-of-function fmr1 mutants carrying an anti-fmr1 miRNA transgene show abnormal neuronal morphology and connectivity similar to that seen in human fragile X syndrome.
FMRP inhibits ADAR2 (Montrer ADARB1 Anticorps) activity, absence of FMRP results in defects of RNA editing of neuronal mRNAs in the mouse model of Fragile X Syndrome.
this study establishes that reducing STEP activity with TC-2153 in Fmr1 KO mice reduces AGS (Montrer GLA Anticorps) susceptibility, improves electrophysiologic and synaptic deficits, and normalizes select social and nonsocial anxiety-related behaviors.
Results indicate several sex-specific changes in Fmr1 knockout mice, including male-specific increases in activity levels, and female-specific increases in repetitive behaviors on both the nose-poke assay and motor coordination on the accelerating rotarod task.
Fmr1 regulates stability of Myf5 (Montrer MYF5 Anticorps) mRNA and skeletal muscle cell renewal.
The results of this study found decreases in either glycinergic or GABAergic inhibition to the medial nucleus of the trapezoid body (MNTB) specific to the tonotopic location within the nucleus in Fmr1 knockout mice.
mGluR5 (Montrer GRM5 Anticorps) was significantly more mobile at synapses in hippocampal Fmr1 KO neurons, causing an increased synaptic surface co-clustering of mGluR5 (Montrer GRM5 Anticorps) and NMDAR (Montrer GRIN1 Anticorps).
The results show that SMNDC1 (Montrer SMNDC1 Anticorps) mRNA 5'-UTR (Montrer UTS2R Anticorps) forms an intramolecular, parallel G quadruplex structure comprised of three G quartet planes, which is bound specifically by FMRP both in vitro and in mouse brain lysates.
Using the Fmr1 null mouse model of fragile X syndrome, brain regions, gene networks, and molecular pathways responsive to a social stimulus have been identified.
This study demonstrated that In vivo recordings from barrel cortex revealed that Fmr1 KO mice show an enlargement in the cortical area activated by whisker deflections.
The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene.
, Fragile-X mental retardation protein
, drosophila fragile X mental retardation protein
, fragile X
, fragile X mental retardation
, fragile X mental retardation 1
, fragile X mental retardation gene
, fragile X mental retardation protein
, fragile X protein
, fragile X related protein
, fragile X-related
, fragile x related
, fragile X mental retardation protein 1
, fragile X mental retardation protein 1 homolog
, fragile X mental retardation syndrome 1 homolog
, fragile X mental retardation-1 protein
, protein FMR-1
, ragile X mental retardation protein
, fragile X mental retardation 1 protein