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Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Additionally we are shipping Histone Deacetylase 5 Antibodies (169) and Histone Deacetylase 5 Kits (10) and many more products for this protein.
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HDAC5 and HDAC6 (show HDAC6 Proteins) were highly expressed in melanoma cells but exhibited low expression levels in normal skin cells.
Formononetin-combined therapy may enhance the therapeutic efficacy of doxorubicin in glioma cells by preventing EMT (show ITK Proteins) through inhibition of HDAC5.
These results suggest a strong regulatory function of HDAC5 in the pro-inflammatory response of macrophages.
In erythroid cells, pull down experiments identified the presence of a novel complex formed by HDAC5, GATA1, EKLF and pERK which was instead undetectable in cells of the megakaryocytic lineage.
Data reveal a novel role of HDAC5 in modulating the KLF2 (show KLF2 Proteins) transcriptional activation and eNOS (show NOS3 Proteins) expression.
Studied phosphorylation sites within functional HDAC5 domains, including the deacetylation domain (DAC (show AADAC Proteins), Ser755), nuclear export signal (NES (show NES Proteins), Ser1108), and an acidic domain (AD, Ser611).
mRNA and protein levels of HDAC5 were up-regulated in human hepatocellular carcinoma.
HDAC5 promoted the Six1 (show SIX1 Proteins) expression.
In C2C12 myoblasts, recombinant human HDAC5 phosphorylation by PKD (show PRKD1 Proteins) regulated the expression of diverse metabolic genes and glucose metabolism.
findings show N-Myc (show MYCN Proteins) upregulated HDAC5 expression in neuroblastoma (show ARHGEF16 Proteins) cells; HDAC5 repressed NEDD4 (show NEDD4 Proteins) gene expression,increased Aurora A (show AURKA Proteins) gene expression and consequently upregulated N-Myc protein (show MYCN Proteins) expression;data identify HDAC5 as a novel co-factor in N-Myc (show MYCN Proteins) oncogenesis
It protects neurons from toxicity of prion (show PRNP Proteins) peptide, and that this protection occurs at through the regulation of the PI3k-Akt (show AKT1 Proteins)-mTOR (show FRAP1 Proteins) axis.
mass spectrometry-based quantitative comparison of acetylated peptides from wild-type vs HDAC6 (show HDAC6 Proteins) knockout mice allowed to identify six new deacetylation sites possibly mediated by HDAC6 (show HDAC6 Proteins).
We therefore tested that reducing HDAC6 (show HDAC6 Proteins) levels by genetic manipulation would attenuate early cognitive and behavioral deficits in R6/1 mice
HDAC6 plays an important role in the function of CMA pathway under the HI stress induced by SCI and it may be a potential therapeutic target in acute SCI model.
inhibition of HDAC5 differentially regulates ghrelin (show GHRL Proteins) and NUCB2/ nesfatin-1 (show NUCB2 Proteins) expression by enhancing the acetylation and phosphorylation of Raptor (show RPTOR Proteins), which subsequently suppress mTORC1 signaling
Results suggest a role for Hdac5 and Sirt2 (show SIRT2 Proteins) in neuronal adaptations induced by chronic stress and antidepressant treatment and highlight the therapeutic potential of these targets in the treatment of depression
loss of HDAC5 weakens Treg suppressive function and iTreg formation, as well as IFN-gamma (show IFNG Proteins) production in CD8 (show CD8A Proteins)+ T cells. Mice lacking HDAC5 do not develop spontaneous illness and do not have enhanced anti-tumor immunity.
functional loss or suppression of the tumor suppressor HDAC6 (show HDAC6 Proteins) is caused by induction of miR (show MLXIP Proteins)-221 through coordinated JNK/c-Jun- and NF-kappaB (show NFKB1 Proteins)-signaling pathways during liver tumorigenesis
Hyperacetylation of Hsp90 (show HSP90 Proteins) is a predictor and causal molecular determinant of stress resilience in mice. Brain-penetrant histone deacetylase 6 (show HDAC6 Proteins) inhibitors increase Hsp90 (show HSP90 Proteins) acetylation and modulate GR chaperone dynamics.
Soluble beta-amyloid disrupts actin and microtubule dynamics via activation of RhoA (show RHOA Proteins) and inhibition of histone deacetylase 6 (show HDAC6 Proteins) in cultured hippocampal neurons.
Protein kinase D-HDAC5 pathway plays an important role in VEGF regulation of gene transcription and angiogenesis
Regulation of flowering time by the histone deacetylase HDA5
Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to the class II histone deacetylase/acuc/apha family. It possesses histone deacetylase activity and represses transcription when tethered to a promoter. It coimmunoprecipitates only with HDAC3 family member and might form multicomplex proteins. It also interacts with myocyte enhancer factor-2 (MEF2) proteins, resulting in repression of MEF2-dependent genes. This gene is thought to be associated with colon cancer. Two transcript variants encoding different isoforms have been found for this gene.
histone deacetylase 5
, antigen NY-CO-9
, histone deacetylase 4
, histone deacetylase mHDA1
, histone deacetylase mHDA2
, scurfy candidate 6