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Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Zusätzlich bieten wir Ihnen Histone Cluster 3, H3 Antikörper (74) und Histone Cluster 3, H3 Kits (2) und viele weitere Produktgruppen zu diesem Protein an.
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Data suggest TCF19 (zeige TCF19 Proteine) interacts with histone 3 lysine 4 trimethylation through its plant homeodomain finger; TCF19 (zeige TCF19 Proteine) expression appears to regulate gluconeogenesis in hepatocytes; TCF19 (zeige TCF19 Proteine) interacts with CHD4 (zeige CHD4 Proteine) causing NuRD complex recruitment to gene promoters of enzymes involved in gluconeogenesis. (TCF19 (zeige TCF19 Proteine) = transcription factor 19 (zeige TCF19 Proteine); CHD4 (zeige CHD4 Proteine) = chromodomain helicase DNA binding protein 4 (zeige CHD4 Proteine); NuRD = nucleosome-remodeling-deacetylase)
Data suggest that, during monocyte-into-macrophage differentiation, extensive trimethylation of histone H3 lysine 4 as well as histone H3 lysine 27 promotes occupancy of histone H3 at promoters of transcription factors such as HOXA (homeodomain proteins) and FOXO (forkhead transcription factors).
Data suggest post-translational modifications of histones, trimethylation of lysine 36 in H3 (H3K36me3) and acetylation of lysine 16 in H4 (H4K16ac), have roles in DNA damage repair; H3K36me3 stimulates H4K16ac upon DNA double-strand break; SETD2, LEDGF (zeige PSIP1 Proteine), and KAT5 (zeige KAT5 Proteine) are required for these epigenetic changes. (SETD2 = SET domain containing 2; LEDGF (zeige PSIP1 Proteine) = lens epithelium-derived growth factor (zeige PSIP1 Proteine); KAT5 (zeige KAT5 Proteine) = lysine acetyltransferase 5 (zeige KAT5 Proteine))
Data show that tet oncogene family member 2 (TET2) cysteine-rich (CR) domain mutations disrupt the recognition of histone H3 lysine 36 (H3K36) methylation, its cellular localization, and enzyme activity.
Screening for H3.3 G34 (zeige GAST Proteine) mutation should therefore be recommended as a routine diagnostic marker for supratentorial central nervous system tumors
Regulators of the histone H3-trimethyl lysine-4 (H3K4me3) mark are significantly associated with the genetic risk architecture of common neurodevelopmental disease.
EP400 deposits H3.3 into chromatin alongside H2AZ and contributes to gene regulation after Pol II pre-initiation complex assembly.
Concurrent acetylation and methylation at H3K27 occurs in hepatocellular carcinoma cells in association with p53 (zeige TP53 Proteine) abnormalities.
TIP60 (zeige KAT5 Proteine) interacted with H3K4me3 in response to TNF-alpha (zeige TNF Proteine) signaling.
Our data highlights the complex interplay between Nrf2 (zeige GABPA Proteine) and H3S10 phosphorylation in arsenite-activated HO-1 (zeige HMOX1 Proteine) transcription.
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a member of the histone H3 family. Transcripts from this gene lack polyA tails\\\\; instead, they contain a palindromic termination element. This gene is located separately from the other H3 genes that are in the histone gene cluster on chromosome 6p22-p21.3.
H3 histone family, member T
, histone 3, H3
, histone H3.1t
, histone cluster 3, H3