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anti-Human Retinoblastoma Binding Protein 4 Antibodies:
anti-Mouse (Murine) Retinoblastoma Binding Protein 4 Antibodies:
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Human Monoclonal Retinoblastoma Binding Protein 4 Primary Antibody for ChIP, ICC - ABIN445503
Humphrey, Wang, Russanova, Hirai, Qin, Nakatani, Howard: Stable histone deacetylase complexes distinguished by the presence of SANT domain proteins CoREST/kiaa0071 and Mta-L1. in The Journal of biological chemistry 2001
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Human Monoclonal Retinoblastoma Binding Protein 4 Primary Antibody for BP, ChIP - ABIN152949
Nicolas, Morales, Magnaghi-Jaulin, Harel-Bellan, Richard-Foy, Trouche: RbAp48 belongs to the histone deacetylase complex that associates with the retinoblastoma protein. in The Journal of biological chemistry 2000
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Human Polyclonal Retinoblastoma Binding Protein 4 Primary Antibody for ICC, IF - ABIN253017
Alvarez-Chaver, Rodríguez-Piñeiro, Rodríguez-Berrocal, García-Lorenzo, Páez de la Cadena, Martínez-Zorzano: Selection of putative colorectal cancer markers by applying PCA on the soluble proteome of tumors: NDK A as a promising candidate. in Journal of proteomics 2011
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The binding interface between AEBP and RBBP4 is relatively small compared with PHF6, histone H3 and FOG-1, indicating that AEBP may not have been the only region that participates in RBBP4 recognition.
RBBP4 forms a negatively charged channel that binds to ZNF827 through a network of electrostatic interactions.
ARMC12 promotes neuroblastoma progression through interaction with RBBP4.
BCL11A interacts with histone methyltransferase (PRC2) and histone deacetylase (NuRD and SIN3A) complexes through their common subunit, RBBP4/7.
RBAP48 overexpression contributes to the radiosensitivity of AGS gastric cancer cells via phosphoinositide3-kinase/protein kinase B pathway suppression.
The MTA1 subunit of the nucleosome remodeling and deacetylase complex can recruit two copies of RBBP4/RBBP7.
RbAp48 is likely to act as a potent antiretroviral defense.
The crystal structure reveals an extensive interface between MTA1 and RBBP4.
RBBP4 interacts with ep300 protein to form a complex that drives the expression of methylguanine-DNA-methyltransferase , RAD51, and other selected DNA repair genes through histone acetylation.
RbAp48 was identified as critical in the proliferation of hypopharyngeal carcinoma in both in vitro and in vivo experiments.
RBBP4 functions as a novel regulatory factor to increase the efficiency of importin alpha/beta-mediated nuclear import
It is associated with episodic memory performance.
Our RBBP4-PHF6 complex structure provides insights into the molecular basis of PHF6-NuRD complex interaction and implicates a role for PHF6 in chromatin structure modulation and gene regulation.
Our results reveal that the protein structure does not affect ligand binding, and the top three TCM candidates Bittersweet alkaloid II, Eicosandioic acid, and Perivine might resolve the instability of the RbAp48-FOG1 complex
RbAp48 recognizes MTA1 using the same site that it uses to bind histone H4, showing that assembly into NuRD modulates RbAp46/48 interactions with histones.
The most significant change was an age-related decline in RbAp48, a histone-binding protein that modifies histone acetylation.
study of the interaction of the histone H3-H4 complex with the RbAp48 and their exchange with a second histone chaperone, anti-silencing function protein 1 (ASF1); exchange of histones H3-H4 between these two histone chaperones has a central role in the assembly of new nucleosomes
Data identified RBBP4 and RBBP9 as required for maintenance of multiple PS cell types, and both RBBPs were bound to RB in PS cells.
The FOG-1 peptide contacts a negatively charged binding pocket on top of the RbAp48 beta-propeller that is distinct from the binding surface used by RpAp48 to contact histone H4
Upergulation of CAF-1 p48 subunit by overexpression of tuberous sclerosis gene products.
Results of genetic interaction analyses revealed that Mi-2 and Caf1/p55, components of the Nucleosome Remodeling and Deacetylase (NuRD) complex, genetically antagonize the role of DREF in germline stem cell maintenance. Taken together, these data suggest that DREF contributes to intrinsic components of the germline stem cell regulatory network that maintains competence to self-renew.
CCR4 and CAF1, the two deadenylases in the CCR4-NOT complex, can remove 3' terminal non-A residues in an exonucleolytic manner.
CAF1-p180 and CAF1-p75 subunits mediate assembly of two different forms of chromatin.
CAF-1 promotes Notch signaling through epigenetic control of target gene expression during Drosophila development.
these studies suggest that p55 is not crucial for PRC2-mediated gene silencing in vivo, and the vital function of p55 is probably not dependent on its interaction with histone H4.
Chromatin-modifying complex component Nurf55/p55 associates with histones H3 and H4 and polycomb repressive complex 2 subunit Su(z)12 through partially overlapping binding sites.
analysis of Caf1 mutant tissue suggests that Caf1 plays important roles in cell survival and segment identity, and loss of Caf1 is associated with a reduction in the Polycomb Repressive Complex 2 (PRC2)-specific histone methylation mark H3K27me3
spreading of heterochromatin is compromised in flies that have reduced CAF-1 p180. Furthermore, reduced CAF-1 p180 causes a defect in the dynamics of heterochromatic markers in early Drosophila embryos.
sliding model in which the position-specific tethering of NURF forces a translocating ISWI ATPase to pump a DNA distortion over the histone octamer, thereby changing the translational position of the nucleosome.
Data show that removal of p55 deregulated the expression of E2F targets that are normally repressed by dE2F2/RBF-1 and -2 complexes in a cell cycle-independent manner but had no effect on the expression of targets normally coupled with cell proliferation.
The nucleosome-binding subunits Su(z)12 and Nurf55 anchor the E(z) enzyme on chromatin substrates, an essential process in maintaining HOX gene silencing during development.
A Pcl-PSC2 complex is the histone methyltransferase that generates the high levels of histone3-lysine27 trimethylation in Polycomb target genes that are needed to maintain a Polycomb-repressed chromatin state.
Results establish that dCAF-1-p180 is an essential gene for Drosophila development and further underscore the importance of dCAF-1 in regulating gene expression and DNA repair in vivo.
Structural basis of histone H4 recognition by p55.
larval endocycling cells lacking CAF-1 large subunit exhibit normal dynamics of progression through endocycles, although accumulating defects, such as perturbation of nucleosomal organisation, reduction of DNA replication and accumulation of DNA damage
results suggest that the ISWI-containing NURF complex functions as a co-activator of Armadillo to promote Wg-mediated transcription.
activation of the OCN/GPR158 pathway increases the expression of RbAp48 in the aged dentate gyrus and rescues age-related memory loss.
RBBP4 is a regulator of histone deacetylation during oocyte maturation and deacetylation is required for bipolar spindle assembly through Aurora kinase C
Studies indicate that estrogen deficiency initiates tissue-specific apoptosis in the exocrine gland cells through RbAp48 overexpression.
Estrogen deficiency initiates p53-mediated apoptosis in the exocrine glands through Rbbp4 overexpression.
Results report that transgenic expression of RbAp48 resulted in the development of autoimmune exocrinopathy resembling Sjogren's syndrome.
rbbp4 is required for survival of postmitotic precursors, and hdac1 maintains proliferation of the neural stem cell/progenitor pool.
This gene encodes a ubiquitously expressed nuclear protein which belongs to a highly conserved subfamily of WD-repeat proteins. It is present in protein complexes involved in histone acetylation and chromatin assembly. It is part of the Mi-2 complex which has been implicated in chromatin remodeling and transcriptional repression associated with histone deacetylation. This encoded protein is also part of co-repressor complexes, which is an integral component of transcriptional silencing. It is found among several cellular proteins that bind directly to retinoblastoma protein to regulate cell proliferation. This protein also seems to be involved in transcriptional repression of E2F-responsive genes. Three transcript variants encoding different isoforms have been found for this gene.
CAF-1 subunit C
, CAF-I 48 kDa subunit
, CAF-I p48
, MSI1 protein homolog
, chromatin assembly factor 1 subunit C
, chromatin assembly factor I p48 subunit
, chromatin assembly factor/CAF-1 p48 subunit
, histone-binding protein RBBP4
, nucleosome-remodeling factor subunit RBAP48
, retinoblastoma-binding protein 4
, retinoblastoma-binding protein p48
, chromatin assembly Factor-1
, chromatin assembly factor 1
, chromatin assembly factor 1 subunit
, chromatin associated factor-1 subunit
, nucleosome remodeling factor
, nucleosome remodeling factor - 55kD
, CAF-1 p48 subunit
, chCAF-1 p48
, chromatin assembly factor 1 p48 subunit
, retinoblastoma binding protein 4
, histone-binding protein RBBP4-A
, retinoblastoma A associated protein
, retinoblastoma-binding protein 4-A
, retinoblastoma-binding protein p48-A