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Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Additionally we are shipping Histone Deacetylase 7 Proteins (13) and Histone Deacetylase 7 Kits (9) and many more products for this protein.
Showing 10 out of 171 products:
Human Polyclonal HDAC7 Primary Antibody for EIA, WB - ABIN356651
Meinke, Liberator: Histone deacetylase: a target for antiproliferative and antiprotozoal agents. in Current medicinal chemistry 2001
Show all 3 references for ABIN356651
Human Polyclonal HDAC7 Primary Antibody for IP, IHC - ABIN223302
Mao, Hou, Cao, Wang, Li, Chen, Fei, Hurren, Gronda, Wu, Trudel, Schimmer: The tricyclic antidepressant amitriptyline inhibits D-cyclin transactivation and induces myeloma cell apoptosis by inhibiting histone deacetylases: in vitro and in silico evidence. in Molecular pharmacology 2011
This study demonstrated a simple and straightforward method of quantifying proneural/mesenchymal markers in glioblastoma. Of note, HDAC7 expression might be a novel therapeutic target in glioblastoma treatment.
HDAC9 (show HDAC9 Antibodies) promotes tumor formation of glioblastoma via TAZ (show TAZ Antibodies)-mediated EGFR (show EGFR Antibodies) pathway activation.
Data suggest, in chronic hepatitis C virus infection, HDAC9 (histone deacetylase 9 (show HDAC9 Antibodies)) induction in liver regulates hepatic gluconeogenesis and systemic insulin (show INS Antibodies) resistance via deacetylation of FoxO1 (show FOXO1 Antibodies) (Forkhead box O (show FOXO Antibodies) 1) and HDAC3 (histone deacetylase 3 (show HDAC3 Antibodies)).
results indicate that HDAC9 variant rs2107595 may be not associated with IS risk in southern Han Chinese
Data show that miR (show MLXIP Antibodies)-376a and HDAC9 (show HDAC9 Antibodies) expression are inversely correlated in hepatocellular carcinoma and suggest that HDAC9 (show HDAC9 Antibodies)-mediated epigenetic modification may contribute to the down-regulation of the miR (show MLXIP Antibodies)-376 cluster in hepatocellular carcinoma.
identify a new target of ROCK signaling via myosin phosphatase subunit (MYPT1 (show PPP1R12A Antibodies)) and histone deacetylase (show HDAC1 Antibodies) (HDAC7) at the nuclear level
Gene expression studies in peripheral blood mononuclear cells revealed increased mRNA levels of HDAC9 (show HDAC9 Antibodies). Analysis of human atherosclerotic plaques revealed no association between rs2107595 and specific plaque characteristics.
Study identifies the miR (show MLXIP Antibodies)-34a-HDAC1 (show HDAC1 Antibodies)/HDAC7-HSP70 (show HSP70 Antibodies) K246 axis as a novel molecular signature predictive of therapy resistance.
The transcriptional function of HCS (show HLCS Antibodies) was shown by in vitro pull down and in vivo co-immunoprecipitation assays to depend on its interaction with the histone deacetylases HDAC1 (show HDAC1 Antibodies), HDAC2 (show HDAC2 Antibodies) and HDAC7
The hydroxamic acid pan (show SUPT6H Antibodies)-HDAC (show HDAC3 Antibodies) inhibitor TSA (show PRDX2 Antibodies) synergistically inhibit the viability.
This study demonstrated that hdac7 decrease in skeletal muscle in muscle atrophy.
HDAC7 in osteoclasts is an important molecular regulator of MITF (show MITF Antibodies) activity and bone homeostasis.
Hdac7 degradation enhances beta-catenin (show CTNNB1 Antibodies) transcriptional activity in growth plate chondrocytes.
In hepatic stellate cells, CYLD (show CYLD Antibodies) removed HDAC7 from the hepatocyte growth factor (show HGF Antibodies) promoter and induced HGF (show HGF Antibodies) expression.
Histone deacetylase 7 promotes Toll-like receptor 4 (show TLR4 Antibodies)-dependent proinflammatory gene expression in macrophages.
HDAC7 overexpression suppresses, whereas HDAC7 deletion enhances, osteoclastogenesis
Nuclear export of histone deacetylase 7 during thymic selection is required for immune self-tolerance
Splicing of histone deacetylase 7 modulates smooth muscle cell proliferation and neointima formation through nuclear beta-catenin (show CTNNB1 Antibodies) translocation.
Data suggest that HDAC7 nuclear export governs a self-sustaining autoexcitatory loop.
Data indicate that CTLs had high expression of the histone deacetylase (show HDAC1 Antibodies) HDAC7 but continually phosphorylated and exported this transcriptional repressor from the nucleus.
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 has sequence homology to members of the histone deacetylase family. This gene is orthologous to the Xenopus and mouse MITR genes. The MITR protein lacks the histone deacetylase catalytic domain. It represses MEF2 activity through recruitment of multicomponent corepressor complexes that include CtBP and HDACs. This encoded protein may play a role in hematopoiesis. Multiple alternatively spliced transcripts have been described for this gene but the full-length nature of some of them has not been determined.
histone deacetylase 7
, histone deacetylase 7A
, MEF-2 interacting transcription repressor (MITR) protein
, histone deacetylase 4/5-related protein
, histone deacetylase 7B