Histone Cluster 3, H3 (HIST3H3) ELISA Kits

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 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
HIST3H3 8290 Q16695
Anti-Maus HIST3H3 HIST3H3 260423 P84228
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Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Lieferzeit Preis Details
Human 0.188 ng/mL 78.13 pg/mL - 5000 pg/mL A typical standard curve 96 Tests 13 bis 16 Tage

Weitere ELISA Kits für Histone Cluster 3, H3 Interaktionspartner

Human Histone Cluster 3, H3 (HIST3H3) Interaktionspartner

  1. the H3 K27M mutation was mainly associated with a poorer prognosis in infratentorial gliomas compared with the corresponding H3 wild-type gliomas

  2. H3.3K27M mutant proteins reprogram epigenome by sequestering the PRC2 complex to poised enhancers.

  3. Mutations in histone h3,3 gene K27M and G34R/W are associated with giant cell tumor of the bone

  4. H3K36me3-mediated mismatch repair preferentially protects actively transcribed genes from mutation.

  5. In 2 cases, we identified H3F3A mutation, classically described in pediatric midline gliomas

  6. Data show that phosphatase and tensin homolog (PTEN) interacts with death domain associated protein (DAXX) and, in turn PTEN directly regulates oncogene expression by modulating DAXX-histone H3.3 (H3.3) association on the chromatin.

  7. Data indicate the mechanism for epigenetic regulation in cancer by inducing E3 ubiquitin ligase NEDD4-dependent histone H3 ubiquitination.

  8. the identification of increased expression of H3K27me3 during a patient's clinical course can be helpful for determining whether the tumors are heterochronous

  9. Here, we report that JMJD5, a Jumonji C (JmjC) domain-containing protein, is a Cathepsin L-type protease that mediates histone H3 N-tail proteolytic cleavage under stress conditions that cause a DNA damage response.

  10. Data suggest that Ki-67 antigen proliferative index has important limitations and hhosphohistone H3 (PHH3) is an alternative proliferative marker.

  11. These results identify cytokine-induced histone 3 lysine 27 trimethylation as a mechanism that stabilizes gene silencing in macrophages

  12. This data indicates that, in the early developing human brain, HIST1H3B constitutes the largest proportion of H3.1 transcripts among H3.1 isoforms.

  13. Data suggest TCF19 interacts with histone 3 lysine 4 trimethylation through its plant homeodomain finger; TCF19 expression appears to regulate gluconeogenesis in hepatocytes; TCF19 interacts with CHD4 causing NuRD complex recruitment to gene promoters of enzymes involved in gluconeogenesis. (TCF19 = transcription factor 19; CHD4 = chromodomain helicase DNA binding protein 4; NuRD = nucleosome-remodeling-deacetylase)

  14. This series of 47 diffuse midline gliomas, histone H3-K27M mutation was mutually exclusive with IDH1-R132H mutation and EGFR amplification, rarely co-occurred with BRAF-V600E mutation, and was commonly associated with p53 overexpression, ATRX loss, and monosomy 10. Among these K27M+ diffuse midline gliomas.

  15. Data show that histone chaperone HIRA co-localizes with viral genomes, binds to incoming viral and deposits histone H3.3 onto these.

  16. These experiments showed that PHF13 binds specifically to DNA and to two types of histone H3 methyl tags (lysine 4-tri-methyl or lysine 4-di-methyl) where it functions as a transcriptional co-regulator.

  17. Hemi-methylated CpGs DNA recognition activates UHRF1 ubiquitylation towards multiple lysines on the H3 tail adjacent to the UHRF1 histone-binding site.

  18. We describe, for the first time, the MR imaging features of pediatric diffuse midline gliomas with histone H3 K27M mutation

  19. Approximately 30% of pediatric high grade gliomas (pedHGG) including GBM and DIPG harbor a lysine 27 mutation (K27M) in histone 3.3 (H3.3) which is correlated with poor outcome and was shown to influence EZH2 function.

  20. 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).

Mouse (Murine) Histone Cluster 3, H3 (HIST3H3) Interaktionspartner

  1. SLBP overexpression caused by Fbxo30 depletion results in a remarkable overload of histone H3 on chromosomes that excessively condenses chromosomes and inhibits chromosome segregation. The finding uncovers an unidentified pathway-controlling chromosome segregation and cell progress.

  2. The data indicate that brachyury mediates acetylated H3K27 recruitment through a physical interaction with p300 during the mouse mesoderm development.

  3. Results suggest a critical role of histone-lysine N-methyltransferase Nsd2-mediated histone H3K36 methylation in adipose tissue development and function.

  4. Histone H3.3K27M and Trp53 loss and PDGFRA overexpression accelerates disease onset and increases tumor invasion.

  5. Histone H3 arginine 2 dimethylation lysine 4 trimethylation, not simply H3lysine 4 trimethylation alone, is the mark of active promoters

  6. Hepatic lipid accumulation alters global histone h3 lysine 9 and 4 trimethylation in the peroxisome proliferator-activated receptor alpha network.

  7. Increased levels of decondensed chromatin in both normal progenitor cells and cancer cells are associated with global loss of H3K27me3, which is linked to MYC overexpression.

  8. histone H3 phosphorylation may be a molecular signature of the activated, retinoid-controlled mRARbeta2 gene promoter

  9. differential regulation between gene expression and histone H3 acetylation in the variable regions of the TCRbeta locus

  10. The elimination of H3K79 methylation after fertilization is involved in genomic reprogramming.

  11. Rb effects permanent cell cycle exit in part by maintaining trimethylation of histone H3 lysine 27 (H3K27) on cell cycle genes.

  12. Pygo2 controls pattern of histone H3 hyperacetylation

  13. Here we show that cAMP signaling regulates histone H3 phosphorylation in a cell cycle-dependent fashion, increasing it in quiescent cells but dramatically reducing it in cycling cells

  14. Bmi1, which methylate H3K27, were present on the HSV-1 genome during latency.

Histone Cluster 3, H3 (HIST3H3) Antigen-Profil

Beschreibung des Gens

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an 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 found in the large histone gene cluster on chromosome 6p22-p21.3.

Genbezeichner und Symbole assoziert mit HIST3H3

  • histone cluster 3 H3 (HIST3H3) Antikörper
  • histone cluster 1 H3 family member a (HIST1H3A) Antikörper
  • histone cluster 3, H3 (HIST3H3) Antikörper
  • histone cluster 1, H3f (Hist1h3f) Antikörper
  • H3.2-221 Antikörper
  • H3.4 Antikörper
  • H3/A Antikörper
  • H3/g Antikörper
  • H3FA Antikörper
  • H3FT Antikörper
  • H3t Antikörper
  • Hist1 Antikörper

Bezeichner auf Proteinebene für HIST3H3

H3 histone family, member T , H3/t , histone 3, H3 , histone H3.1t , H3 histone family, member A , histone 1, H3a , histone H3.1 , histone H3/a , histone cluster 3, H3 , histone 1, H3f , histone H3 , histone H3.2 , histone gene complex 1

8290 Homo sapiens
8350 Homo sapiens
480760 Canis lupus familiaris
260423 Mus musculus
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