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NSD1 encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. Additionally we are shipping and many more products for this protein.
Showing 10 out of 39 products:
Human Monoclonal NSD1 Primary Antibody for ELISA, WB - ABIN528606
Lu, Jackson, Wang, Yang, Chance, Miyagi, Gudkov, Stark: Regulation of NF-kappaB by NSD1/FBXL11-dependent reversible lysine methylation of p65. in Proceedings of the National Academy of Sciences of the United States of America 2010
NSD1 mutation is associated with severe connective tissue laxity including aortic dilatation in Sotos syndrome.
NSD1 mutation is associated with Hyperinsulinemic hypoglycemia.
Studies indicate that the NSD methyltransferases NSD1, NSD2/WHSC1/MMSET (show WHSC1 Antibodies) and NSD3/WHSC1L1 (show WHSC1L1 Antibodies) were overexpressed, amplified or somatically mutated in multiple types of cancer, suggesting their critical role in cancer.
The genome-wide impact of a highly significant NSD1(+/-)-specific signature that differentiates pathogenic NSD1 mutations from controls, benign NSD1 variants and the clinically overlapping Weaver (show KCNJ6 Antibodies) syndrome is described.
The results describe the binding of NSD1, 2 and 3 catalytic domains CD) on histone tails through recognition of histone-lysine and methylation properties.
NSD1 interacted with RNAPII and bound to GSTM3 (show glutathione S-transferase mu 3 (brain) Antibodies) -63A/C TATA box.
Acute myeloid leukemia (show BCL11A Antibodies) can be reproduced in mice by transducing mouse mesenchymal stem cells with the human NUP98 (show NUP98 Antibodies)-NSD1 fusion and the FLT3 (show FLT3 Antibodies)-ITD mutated constracts.
This report describes, for the first time, a Korean family with two generations of Stotos syndrome resulting from a novel intragenic NSD1 mutation.
NSD1 prefers aromatic, hydrophobic, and basic residues at the -2, -1 and +2, and +1 sites of its substrate peptide in histone H3 (show HIST3H3 Antibodies).
support to the adoption of screening for NUP98 (show NUP98 Antibodies)-NSD1 in pediatric AML (show RUNX1 Antibodies) without otherwise favorable genetic markers
Silencing of Nsd1 followed by LLO stimulation led to increased caspase-1 (show CASP1 Antibodies) activation, enhanced post-translational maturation of IL-1beta (show IL1B Antibodies) and IL-18 (show IL18 Antibodies) and elevated pyroptosis, a form of cell death associated with inflammation.
Nsd1 contains consensus TFII-I (show GTF2I Antibodies) binding sites in the proximal promoters; the chromatin immunoprecipitation analysis showed that TFII-I (show GTF2I Antibodies) transcription factors are recruited to these sites in vivo in Williams-Beuren syndrome.
all of the H3K36-specific methyltransferases, including ASH1L (show ASH1L Antibodies), HYPB (show SETD2 Antibodies), NSD1, and NSD2 (show WHSC1 Antibodies) were inhibited by ubH2A, whereas the other histone methyltransferases, including PRC2, G9a (show EHMT2 Antibodies), and Pr-Set7 (show SETD8 Antibodies) were not affected by ubH2A.
NSD1 interaction with liganded NRs (show SPNS1 Antibodies) including ERa, AR, RARa (show RARA Antibodies), RXRa (show RXRA Antibodies), TRb (show AATF Antibodies), PPARg (show PPARG Antibodies) and VDR (show CYP27B1 Antibodies) is mediated by an LXXLL motif. Interaction with the NR2E/F subfamily including COUP-TFI (show NR2F1 Antibodies), COUP-TFII (show NR2F2 Antibodies), EAR2 (show NR2F6 Antibodies) and TLX (show NR2E1 Antibodies) requires an overlapping F/YSXXLXXL/Y motif.
Data show that nuclear receptor-binding SET domain-containing protein (NSD1) is a developmental regulatory protein with histone methyltransferase activity that exerts function(s) essential for early post-implantation development.
Nizp1 (show ZNF496 Antibodies) contains a novel type of zinc finger motif that functions as a docking site for NSD1
This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Two transcript variants encoding distinct isoforms have been identified for this gene.
nuclear receptor binding SET domain protein 1
, histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific-like
, NR-binding SET domain-containing protein
, androgen receptor coactivator 267 kDa protein
, androgen receptor-associated coregulator 267
, androgen receptor-associated protein of 267 kDa
, histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific
, lysine N-methyltransferase 3B
, nuclear receptor-binding SET domain-containing protein 1