HDAC1 Antibody (PA1-860) in IFImmunofluorescent analysis of HDAC1 in MCF-7 Cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a HDAC1 polyclonal antibody (Product # PA1-860) at a dilution of 1:100 overnight at 4 C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody (Product # 35552). HDAC1 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.HDAC1 Antibody (PA1-860) in IHCImmunohistochemistry was performed on normal biopsies of deparaffinized human tonsil tissue. To expose target proteins, heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a Rabbit Polyclonal Antibody recognizing HDAC1 (Product # PA1-860) or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP, followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.HDAC1 Antibody (PA1-860) in IFImmunofluorescent analysis of HDAC1 (green) in 3T3 cells. The cells were permeabilized with 0.1% Triton X-100 in TBS for 15 minutes, and blocked with 3% BSA in PBS (Product # 37525) for 15 minutes at room temperature. Cells were stained with a HDAC1 rabbit polyclonal antibody (Product # PA1-860), at a concentration of 10 µg/mL in blocking buffer for at least 1 hour at room temperature, and then incubated with a Goat anti-rabbit IgG Superclonal secondary antibody, Alexa Fluor 488 conjugate (Product # A27034) at a dilution of 1:1000 for 30 minutes at room temperature (green). Nuclei (blue) were stained with Hoechst 33342 dye (Product # 62249). Images were taken on a Thermo Scientific ToxInsight Instrument at 20X magnification. |
1.The Journal of neuroscience : the official journal of the Society for NeuroscienceHDAC1 and HDAC2 control the specification of neural crest cells into peripheral glia."PA1-860 was used in ChIP assay, immunohistochemistry, and western blot to study the roles of Pax3, Sox10 and Fabp7 in the mechanism by which HDAC-1 and -2 control the specification of neural crest cells into peripheral glia"AuthorsJacob C,Lötscher P,Engler S,Baggiolini A,Varum Tavares S,Brügger V,John N,Büchmann-Møller S,Snider PL,Conway SJ,Yamaguchi T,Matthias P,Sommer L,Mantei N,Suter U2.LeukemiaChromatin modifications induced by the AML1-ETO fusion protein reversibly silence its genomic targets through AML1 and Sp1 binding motifs."PA1-860 was used in ChIP assay to investigate the importance of Sp1 in functional chromatin modifications induced by AML1-ETO"AuthorsMaiques-Diaz A,Chou FS,Wunderlich M,Gómez-López G,Jacinto FV,Rodriguez-Perales S,Larrayoz MJ,Calasanz MJ,Mulloy JC,Cigudosa JC,Alvarez S3.Journal of virologyTax relieves transcriptional repression by promoting histone deacetylase 1 release from the human T-cell leukemia virus type 1 long terminal repeat."PA1-860 was used in chromatin immunoprecipitation to study the effect of HTLV-1 viral transcriptional activator Tax on transcriptional regulation."AuthorsLu H,Pise-Masison CA,Linton R,Park HU,Schiltz RL,Sartorelli V,Brady JN4.Molecular cellSpecificity in circadian clock feedback from targeted reconstitution of the NuRD corepressor."PA1-860 was used in western blot to investigate how different NuRD subunits regulate the PER complex."AuthorsKim JY,Kwak PB,Weitz CJ5.Neurobiology of agingEffect of high-intensity exercise on aged mouse brain mitochondria, neurogenesis, and inflammation."PA1-860 was used in western blot to determine how intensive exercise affects brain bioenergetics, inflammation, and neurogenesis-relevant parameters"AuthorsE L,Burns JM,Swerdlow RH |