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Human HDAC5 ELISA Kit for Sandwich ELISA - ABIN420524
Alam, Rashid, Kabir, Raqib, Ahmad: On birth single dose live attenuated OPV and BCG vaccination induces gut cathelicidin LL37 responses at 6 week of age: a natural experiment. in Vaccine 2014
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HDAC5 inhibits hepatic lipogenic genes expression by attenuating the transcriptional activity of liver X receptor.
HDAC5 promotes cellular proliferation through the upregulation of cMet, and may provide a novel therapeutic target for the treatment of patients with Wilms' tumor.
HDAC5 and HDAC6 (show HDAC6 ELISA Kits) 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 ELISA Kits) 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 ELISA Kits) transcriptional activation and eNOS (show NOS3 ELISA Kits) expression.
Studied phosphorylation sites within functional HDAC5 domains, including the deacetylation domain (DAC (show AADAC ELISA Kits), Ser755), nuclear export signal (NES (show NES ELISA Kits), 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 ELISA Kits) expression.
As HDAC5 expression may help nullify AIS (show AR ELISA Kits) and identify progenitor cells, the precise delivery of miD2861 may serve as a vehicle for monitoring network remodeling with target specificity and signal sensitivity after drug exposure that identifies brain repair processes in adult animals.
HDAC6 (show HDAC6 ELISA Kits)-mediated autophagy negatively regulates primary cilia length during silibinin treatment and has the potential to serve as a therapeutic target for primary cilia-associated ciliopathies.
HDAC6 (show HDAC6 ELISA Kits) is an effector of the immune cytotoxic response that acts by affecting the dynamics, transport and secretion of lytic granules by cytotoxic T lymphocytes.
This study demonstrated that mice with learned helplessness protocol-induced behavioral despair exhibited higher levels of HDAC5 and HDAC5 binding to the promoter region of BDNF (show BDNF ELISA Kits) exon IV resulting in the decreased expression of BDNF (show BDNF ELISA Kits).
It protects neurons from toxicity of prion (show PRNP ELISA Kits) peptide, and that this protection occurs at through the regulation of the PI3k-Akt (show AKT1 ELISA Kits)-mTOR (show FRAP1 ELISA Kits) axis.
mass spectrometry-based quantitative comparison of acetylated peptides from wild-type vs HDAC6 (show HDAC6 ELISA Kits) knockout mice allowed to identify six new deacetylation sites possibly mediated by HDAC6 (show HDAC6 ELISA Kits).
We therefore tested that reducing HDAC6 (show HDAC6 ELISA Kits) 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 ELISA Kits) and NUCB2/ nesfatin-1 (show NUCB2 ELISA Kits) expression by enhancing the acetylation and phosphorylation of Raptor (show RPTOR ELISA Kits), which subsequently suppress mTORC1 signaling
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