- Suchergebnis für K11405
Cookie-Einstellungen
Diese Website benutzt Cookies, die für den technischen Betrieb der Website erforderlich sind und stets gesetzt werden. Andere Cookies, die den Komfort bei Benutzung dieser Website erhöhen, der Direktwerbung dienen oder die Interaktion mit anderen Websites und sozialen Netzwerken vereinfachen sollen, werden nur mit Ihrer Zustimmung gesetzt.
Konfiguration
Technisch erforderlich
Diese Cookies sind für die Grundfunktionen des Shops notwendig.
"Alle Cookies ablehnen" Cookie
"Alle Cookies annehmen" Cookie
Ausgewählter Shop
CSRF-Token
Cookie-Einstellungen
FACT-Finder Tracking
Individuelle Preise
Kundenspezifisches Caching
Session
Währungswechsel
Komfortfunktionen
Diese Cookies werden genutzt um das Einkaufserlebnis noch ansprechender zu gestalten, beispielsweise für die Wiedererkennung des Besuchers.
Facebook-Seite in der rechten Blog - Sidebar anzeigen
Merkzettel
Statistik & Tracking
Endgeräteerkennung
Kauf- und Surfverhalten mit Google Tag Manager
Partnerprogramm
Zu "K11405" wurden 50 Artikel gefunden!
Filter schließen
Filtern nach:
Für die Filterung wurden keine Ergebnisse gefunden!
Artikelnummer: BPS-50008
Active humanHDAC8 , GenBank Accession No. NM_018486, full length with C-terminal His tag, MW= 42.4 kDa, expressed in a baculovirus expression system.
Schlagworte: | HD8, CDA07, HDACL1, Histone deacetylase 8, Protein deacetylase HDAC8, Protein decrotonylase HDAC8, |
Anwendung: | Enzyme kinetics, inhibitor screening |
MW: | 42.4 kD |
679,00 €
Artikelnummer: Cay10444-10
PCI 34051 is a potent histone deacetylase (HDAC) 8 inhibitor (IC50 = 0.01 µM) with >200-fold selectivity over HDAC isoforms 1, 2, 3, 6, and 10 (IC50s = 4, >50, >50, 2.9, and 13 µM, respectively). PCI 34051 induces caspase-dependent apoptosis in cell lines derived from T-cell lymphomas or leukemias (GI50s = 2.4 - 4...
Schlagworte: | N-hydroxy-1-[(4-methoxyphenyl)methyl]-1H-indole-6-carboxamide |
Anwendung: | HDAC inhibitor |
CAS | 950762-95-5 |
MW: | 296.3 D |
ab 104,00 €
Artikelnummer: Cay17130-500
Romidepsin, also known as FK228, is a natural bicyclic depsipeptide that, following reduction, selectively inhibits class I histone deacetylases (HDACs). Reduction of a disulfide bond on romidepsin within the cell generates a zinc-binding thiol, allowing potent and selective inhibition of HDAC1, 2, 3, and 8 (IC50s =...
Schlagworte: | FK228, FR901228, NSC 630176, cyclic... |
Anwendung: | Class I HDAC inhibitor |
CAS | 128517-07-7 |
MW: | 540.7 D |
ab 147,00 €
Artikelnummer: Cay19380-50
Histone deacetylase 8 (HDAC8) is a class I HDAC that catalyzes the zinc-dependent deacetylation of core histones. It is composed of a single alpha/beta domain with an N-terminal deacetylase active site, which can be disrupted by phosphorylation of a proximal serine. HDAC8 is ubiquitously expressed in human tissues...
Schlagworte: | HD8, HD8, HDAC8, CDA07, HDACL1, Histone deacetylase 8, Histone deacetylase 8 |
Anwendung: | Enzyme activity |
MW: | 45,3 kD |
571,00 €
Artikelnummer: Cay700230-96
Human HDAC8 is a class I HDAC and has been identified in a variety of human cancer tissues. Cayman's HDAC8 Inhibitor Screening Assay provides a convenient fluorescence-based method for screening HDAC8 inhibitors. The procedure requires only two easy steps, both performed in the same microplate. The fluorescent...
Schlagworte: | Histone Deacetylase 8 Inhibitor Screening Assay Kit |
Anwendung: | HDAC8 inhibitor screening |
Spezies-Reaktivität: | human |
467,00 €
Artikelnummer: BPS-50068
The Fluorogenic HDAC8 Assay Kit is a complete assay system designed to measure histone deacetylases 8 (HDAC8) activity in cell extracts, nuclear extracts, immunoprecipitates, and purified enzymes. It comes in a convenient 96-well format, with all the reagents necessary for fluorescent HDAC activity measurements. In...
Schlagworte: | HD8, CDA07, HDACL1, Histone deacetylase 8, Protein deacetylase HDAC8, Protein decrotonylase HDAC8, |
Anwendung: | HDAC8 assays, inhibitor screening, HTS |
657,00 €
Artikelnummer: Cay21273-5
UF010 is a class I HDAC inhibitor with IC50 values of 0.06, 0.1, 0.5, and 1.5 µM for HDAC3, 2, 1, and 8, respectively. It is more than 6-fold selective for these class I HDACs over any additional HDACs. UF010 is reported to inhibit cancer cell proliferation with a mean GI50 value of 2.94 µM when screened against the...
Schlagworte: | 4-bromo-benzoic acid, 2-butylhydrazide |
Anwendung: | Class I HDAC inhibitor |
CAS | 537672-41-6 |
MW: | 271.2 D |
ab 60,00 €
Artikelnummer: Cay28832-10
HDAC8-IN-1 is an inhibitor of histone deacetylase 8 (HDAC8, IC50 = 27.2 nM). It is selective for HDAC8 over HDAC1-3, -4, -6, -10, and -11 (IC50s = >3,000 nM for all). HDAC8-IN-1 is cytotoxic to A549, H1299, and CL1-5 lung cancer cells (IC50s = 7.9, 7.2, and 7 µM, respectively).Formal Name:...
Schlagworte: | MDK-7933, (2E)-N-hydroxy-3-(5-methoxy[1,1':4',1''-terphenyl]-2-yl)-2-propenamide |
Anwendung: | HDAC8 inhibitor |
CAS | 1417997-93-3 |
MW: | 345.4 D |
ab 60,00 €
Artikelnummer: ARG51629.100
Protein function: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone...
Schlagworte: | Anti-phospho-HD8, Anti-phospho-CDA07, Anti-phospho-HDAC8, Anti-phospho-HDACL1, EC=3.5.1.98, Anti-phospho-Histone... |
Anwendung: | ICC, IF, IHC (paraffin) |
Wirt: | Rabbit |
Spezies-Reaktivität: | human, mouse, rat |
ab 436,00 €
Artikelnummer: G-HUFI00995.96
Anwendung: | ELISA |
Spezies-Reaktivität: | human |
641,00 €
Artikelnummer: NSJ-R30669
0.5mg/ml if reconstituted with 0.2ml sterile DI water. Histone deacetylase 8 is an enzyme that in humans is encoded by the HDAC8 gene, and is biologically involved in skull morphogenesis and metabolic control of the ERR-alpha/PGC1-alpha transcriptional complex. Sequence analysis predicted that the 377-amino acid...
Schlagworte: | Anti-HD8, Anti-HDAC8, Anti-CDA07, Anti-HDACL1, EC=3.5.1.98, Anti-Histone deacetylase 8, HDAC8 Antibody |
Anwendung: | WB, IHC (paraffin) |
Wirt: | Rabbit |
Spezies-Reaktivität: | human, mouse, rat |
755,00 €
Artikelnummer: BPS-27620-1
Droxinostat is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 ?M and 1.46 ?M, greater than 8-fold selective against HDAC3 and no inhibition to HDAC1, 2, 4, 5, 7, 9, and 10.
Schlagworte: | NS 41080, 4-(4-Chloro-2-methylphenoxy)-N-hydroxybutanamide, |
Anwendung: | HDAC6/8 inhibitor |
MW: | 243.7 D |
ab 350,00 €