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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
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
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.
The minor allele A of SNP rs2107595 increased coronary artery disease risk and the severity of coronary atherosclerosis in a Chinese Han population.
in leiomyosarcomas (LMS), this two-faced trait of MEF2 (show MEF2A Antibodies) is relevant for tumor aggressiveness. Class IIa HDACs are overexpressed in 22% of LMS, where high levels of MEF2 (show MEF2A Antibodies), HDAC4 (show HDAC4 Antibodies) and HDAC9 (show HDAC9 Antibodies) inversely correlate with overall survival. The knock out of HDAC9 (show HDAC9 Antibodies) suppresses the transformed phenotype of LMS cells, by restoring the transcriptional proficiency of some MEF2 (show MEF2A Antibodies)-target loci
Based on this study, it is suggested that HDAC9 regulates the formation of APBs and could be a candidate for the target of ALT-cancer therapy.
PC3/Tis21 (show BTG2 Antibodies) associates with HDAC1 (show HDAC1 Antibodies), HDAC4 (show HDAC4 Antibodies), and HDAC9 (show HDAC9 Antibodies) in vivo, in fibroblast cells.
HDAC9 (show HDAC9 Antibodies) is a target of miR (show MLXIP Antibodies)-377 in oral squamous cell carcinoma.
Studied HDAC9 gene's association with an increased susceptibility to acute coronary syndrome (ACS) in Chinese Han population. The results revealed a significant association of rs2240419 with ACS risk in which the A allele (P = 0.047) and the A allele carriers (AA + AG) (P = 0.037) were more likely to be in ACS group as compared to those in the control group.
Downregulation of HDAC9 (show HDAC9 Antibodies) promotes gliomas.
overexpression of HDAC9 (show HDAC9 Antibodies) contributes to OSCC carcinogenesis via targeting a transcription factor, MEF2D (show MEF2D Antibodies), and NR4A1/Nur77 (show NR4A1 Antibodies), a pro-apoptotic MEF2 (show MEF2A Antibodies) target
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.
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.
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