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抗Human PRMT7 抗体:
抗Rat (Rattus) PRMT7 抗体:
抗Mouse (Murine) PRMT7 抗体:
Human Polyclonal PRMT7 Primary Antibody for ChIP, ICC - ABIN4347365
Blanc, Vogel, Chen, Crist, Richard: PRMT7 Preserves Satellite Cell Regenerative Capacity. in Cell reports 2016
Human Polyclonal PRMT7 Primary Antibody for ELISA, WB - ABIN4347366
Lee, Cook, Yang, Mirochnitchenko, Gunderson, Felix, Herth, Hoffmann, Pestka: PRMT7, a new protein arginine methyltransferase that synthesizes symmetric dimethylarginine. in The Journal of biological chemistry 2005
These kinetic studies suggest a biochemical explanation for the interplay between PRMT5 (显示 PRMT5 抗体)- and PRMT7-mediated methylation of the same substrate at different residues and also suggest a general model for regulation of PRMTs.
The authors showed that ASS1 (显示 ASS1 抗体) mutations linked to type I citrullinemia (显示 ASS1 抗体) disrupt the ASS1 (显示 ASS1 抗体)-PRMT7 interaction, which might explain the molecular pathogenesis of the disease.
Loss of PRMT7 causes decreases in arginine methylation throughout the proteome.Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly.
Upregulation of PRMT7 in breast cancer may have a significant role in promoting cell invasion through the regulation of MMP9 (显示 MMP9 抗体).
results define PRMT7 as an inducer of breast cancer metastasis and present the opportunity for applying PRMT7-targeted therapeutics to treat highly invasive breast cancers
Data indicate that two acidic residues within the double E loop, Asp (显示 ASIP 抗体)-147 and Glu (显示 DCTN1 抗体)-149, confer specificity to protein arginine methyltransferase 7 (PRMT7.
reducing expression of individual PRMT7 target DNA repair genes showed that only the catalytic subunit of DNA polymerase (显示 POLB 抗体), POLD1 (显示 POLD1 抗体), was able to resensitize PRMT7 knock-down cells to DNA-damaging agents.
Human protein arginine methyltransferase 7 (PRMT7) is a type III enzyme forming omega-NG-monomethylated arginine residues.
Here the authors report that H3R2 is also symmetrically dimethylated (H3R2me2s) by PRMT5 (显示 PRMT5 抗体) and PRMT7 and present in euchromatic regions.
PRMT7 (like PRMT5 (显示 PRMT5 抗体)) is a Type II methyltransferase capable of producing symmetric dimethylarginine modifications in proteins.
Of the 28 proteins, only arginine methyltransferase 7 (PRMT7) changed substantially during mouse embryogenesis and promoted the conversion of mouse fibroblasts into iPSCs. Specifically, PRMT7 replaced SOX2 (显示 SOX2 抗体) in a factor-substitution assay, yielding iPSCs
miR (显示 MLXIP 抗体)-24-2-5p is an anti-pluripotent miRNA involved in a novel epigenetic stemness-regulatory mechanism in which a double-negative feedback loop consisting of PRMT7 and miR (显示 MLXIP 抗体)-24-3p/miR24-2-5p interplays with Oct4 (显示 POU5F1 抗体), Nanog (显示 NANOG 抗体), Klf4 (显示 KLF4 抗体) and c-Myc (显示 MYC 抗体) to control stemness.
Prmt7 is a key regulator for skeletal muscle oxidative metabolism. Prmt7 is expressed at the highest levels in skeletal muscle and decreased in skeletal muscles with age or obesity. Prmt7(-/-) muscles exhibit decreased oxidative metabolism with decreased expression of genes involved in muscle oxidative metabolism, including PGC-1alpha. Consistently, Prmt7(-/-) mice exhibited significantly reduced endurance exercise cap...
The findings define PRMT7 as a regulator of the DNMT3b (显示 DNMT3B 抗体)/p21 (显示 D4S234E 抗体) axis required to maintain muscle stem cell regenerative capacity.
PRMT7 structure is composed of two catalytic modules in tandem forming a pseudo-dimer and contains only one AdoHcy molecule bound to the N-terminal module
PRMT7 could recruit H4R3me1 and symmetric H4R3me2 to the Bcl6 (显示 BCL6 抗体) promoter. These results provide evidence for the important roles played by PRMT7 in germinal center formation.
Mammalian protein arginine methyltransferase 7 (PRMT7) specifically targets RXR sites in lysine- and arginine-rich regions.
CTCFL (显示 CTCFL 抗体) and PRMT7 may play a role in male germline imprinted gene methylation.
Prmt7 regulates epiboly by facilitating 2-OST and modulating actin cytoskeleton
C. elegans PRMT-7 has a substrate specificity and a substrate preference different from those of mammalian PRMT7, and the available X-ray crystal structures of the PRMT7 orthologs show differences in active site architecture
Data indicate that only the N-terminal catalytic site of protein arginine methyltransferase 7 (PRMT7) is responsible for cofactor binding.
Arginine methylation is an apparently irreversible protein modification catalyzed by arginine methyltransferases, such as PMT7, using S-adenosylmethionine (AdoMet) as the methyl donor. Arginine methylation is implicated in signal transduction, RNA transport, and RNA splicing (Miranda et al., 2004
protein arginine methyltransferase 7
, [Myelin basic protein]-arginine N-methyltransferase PRMT7
, histone-arginine N-methyltransferase PRMT7
, myelin basic protein-arginine N-methyltransferase
, protein arginine N-methyltransferase 7
, arginine N-methyltransferase
, Histone-arginine N-methyltransferase PRMT7