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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
Human Polyclonal HDAC7 Primary Antibody for ICC, IF - ABIN4316779
Murata, Yoshimoto, Hatae, Akagi, Mizoguchi, Hata, Kuga, Nakamizo, Amano, Sayama, Iihara: Detection of proneural/mesenchymal marker expression in glioblastoma: temporospatial dynamics and association with chromatin-modifying gene expression. in Journal of neuro-oncology 2015
Human Monoclonal HDAC7 Primary Antibody for RNAi, ELISA - ABIN565634
Malik, Jiang, Garee, Verdin, Lee, OMalley, Zhang, Belaguli, Oesterreich: Histone deacetylase 7 and FoxA1 in estrogen-mediated repression of RPRM. in Molecular and cellular biology 2009
Study found increased HDAC7 expression in human pancreatic islets from type 2 diabetic compared with non-diabetic donors. HDAC7 expression correlated negatively with insulin (show INS Antibodies) secretion in human islets.
silencing HDAC7 can reset the tumor suppressor activity of STAT3 (show STAT3 Antibodies), independently of the EGFR (show EGFR Antibodies)/PTEN (show PTEN Antibodies)/TP53 (show TP53 Antibodies) background of the glioblastoma.
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.
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
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
endothelial progenitor cells involved in the angiogenesis might be controlled by VEGF (show VEGFA Antibodies)-PKD1 (show PKD1 Antibodies)-HDAC7 axis, which regulates the EPCs angiogenesis by PKD1 (show PKD1 Antibodies), but not the ERK (show EPHB2 Antibodies) and PI3K (show PIK3CA Antibodies) pathway
Histone deacetylase 7 promotes Toll-like receptor 4 (show TLR4 Antibodies)-dependent proinflammatory gene expression in macrophages.
Expression of JHDM2A (show KDM3A Antibodies) was significantly increased but HDAC2 (show HDAC2 Antibodies), HDAC7, and SUV39H2 (show SUV39H2 Antibodies) were significantly down-regulated in Systemic Sclerosis B cells relative to controls
Authors identified acetyltransferase p300 (show EP300 Antibodies) and deacetylase HDAC7 as enzymes modulating human T cell leukemia virus type 1 Tax (show CNTN2 Antibodies) protein acetylation.
HDAC7 is a bona fide transcriptional repressor essential for B cell development.
In the dorsal hippocampus, HDAC7 expression is decreased following contextual fear conditioning.
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.
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.
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 mouse HDAC7 gene whose protein promotes repression mediated via the transcriptional corepressor SMRT. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
, histone deacetylase 7A
, histone deacetylase 7