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This locus encodes a nuclear matrix protein. Zusätzlich bieten wir Ihnen Matrin 3 Kits (11) und Matrin 3 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 72 products:
Human Polyclonal MATR3 Primary Antibody für ICC, IF - ABIN151288
Schessl, Zou, McGrath, Cowling, Maiti, Chin, Sewry, Battini, Hu, Cottle, Rosenblatt, Spruce, Ganguly, Kirschner, Judkins, Golden, Goebel, Muntoni, Flanigan, Mitchell, Bönnemann: Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy. in The Journal of clinical investigation 2008
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Cow (Bovine) Polyclonal MATR3 Primary Antibody für IHC, WB - ABIN2779141
Beausoleil, Jedrychowski, Schwartz, Elias, Villén, Li, Cohn, Cantley, Gygi: Large-scale characterization of HeLa cell nuclear phosphoproteins. in Proceedings of the National Academy of Sciences of the United States of America 2004
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Human Polyclonal MATR3 Primary Antibody für ICC, IF - ABIN151103
Dunham-Ems, Lee, Stachowiak, Pudavar, Claus, Prasad, Stachowiak: Fibroblast growth factor receptor-1 (FGFR1) nuclear dynamics reveal a novel mechanism in transcription control. in Molecular biology of the cell 2009
Human Polyclonal MATR3 Primary Antibody für ICC, IF - ABIN4332842
Johnson, Pioro, Boehringer, Chia, Feit, Renton, Pliner, Abramzon, Marangi, Winborn, Gibbs, Nalls, Morgan, Shoai, Hardy, Pittman, Orrell, Malaspina, Sidle, Fratta, Harms, Baloh, Pestronk, Weihl et al.: Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. ... in Nature neuroscience 2014
Using a novel RNA pulldown approach that utilized endogenous S1-tagged PINCR (a p53 (zeige TP53 Antikörper)-regulated long noncoding RNA), the authors show that PINCR associates with the enhancer region of these genes by binding to RNA-binding protein (zeige PTBP1 Antikörper) Matrin 3 that, in turn, associates with p53 (zeige TP53 Antikörper).
A missense mutation in MATR3 was identified in myopathy patients undergoing a needle electromyography.
Our findings indicate that mutations in Matrin 3 that are associated with ALS and myopathy do not dramatically alter the normal localization of the protein or readily induce inclusion formation.
Three-dimensional mapping of the lamin A (zeige LMNA Antikörper)-matrin-3 interface showed that the LMNA (zeige LMNA Antikörper) truncating mutation Delta303, which lacks the matrin-3 binding domain, was associated with an increased distance between lamin A (zeige LMNA Antikörper) and matrin-3.
Suppressing Matrin 3 powers a heightened and broader ZAP (zeige ZC3HAV1 Antikörper) restriction of HIV-1 gene expression.
MATR3 mutation is identified to be a possible cause of amyotrophic lateral sclerosis.
No mutations were identified, indicating that MATR3 mutations are not a common cause of Amyotrophic lateral sclerosis in Australian familial cases with predominately European ancestry
MATR3 gene disruption is associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus.
Mutations in MATR3 are rare in French familial ALS and ALS with FTLD patients.
This study shows a high risk of abnormal respiratory function with progressive worsening in MATR3 myopathy.
Matrin 3 (MATR3) is a novel protein interactor of PABPN1 (zeige PABPN1 Antikörper). MATR3 together with PABPN1 (zeige PABPN1 Antikörper) is required for normal paraspeckle function.
Matrin 3 declines significantly in the central nervous system through early development and young adulthood before stabilizing.
Matr3(Gt-ex13) gene trap insertion disturb the polyadenylation of MATR3 transcripts and alter Matrin 3 protein expression.
Matrin 3 interacts specifically with the heat shock proteins glucose-regulated protein 78 (zeige HSPA5 Antikörper), GRP75 (zeige HSPA9 Antikörper) and glutathione S-transferase (zeige GSTa2 Antikörper) pi isoform 2.
This locus encodes a nuclear matrix protein. Mutations at this locus have been associated with distal myopathy 2, which often includes vocal cord and pharyngeal weakness. Alternatively spliced transcript variants, including read-through transcripts with an upstream locus have been described. Related pseuodgenes have been defined on chr1 and chrX.
, vocal cord and pharyngeal weakness with distal myopathy
, nuclear scaffold protein P130/MAT3
, matrin 3