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This locus encodes a nuclear matrix protein. Additionally we are shipping KIAA1191 Proteins (4) and many more products for this protein.
Showing 10 out of 16 products:
Depletion of SAFB1 (show SAFB Antibodies) reduced FUS's localization to chromatin-bound fraction and splicing activity, suggesting SAFB1 (show SAFB Antibodies) could tether FUS (show FUS Antibodies) to chromatin compartment thorough N-terminal DNA-binding motif. Moreover, FUS (show FUS Antibodies) interacts with another nuclear matrix-associated (show SMARCA5 Antibodies) protein, Matrin3.
Using a novel RNA pulldown approach that utilized endogenous S1-tagged PINCR (a p53 (show TP53 Antibodies)-regulated long noncoding RNA), the authors show that PINCR associates with the enhancer region of these genes by binding to RNA-binding protein (show PTBP1 Antibodies) Matrin 3 (show MATR3 Antibodies) that, in turn, associates with p53 (show TP53 Antibodies).
A missense mutation in MATR3 (show MATR3 Antibodies) 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 (show LMNA Antibodies)-matrin-3 (show MATR3 Antibodies) interface showed that the LMNA (show LMNA Antibodies) truncating mutation Delta303, which lacks the matrin-3 (show MATR3 Antibodies) binding domain, was associated with an increased distance between lamin A (show LMNA Antibodies) and matrin-3 (show MATR3 Antibodies).
Suppressing Matrin 3 (show MATR3 Antibodies) powers a heightened and broader ZAP (show ZC3HAV1 Antibodies) restriction of HIV-1 gene expression.
MATR3 (show MATR3 Antibodies) mutation is identified to be a possible cause of amyotrophic lateral sclerosis.
No mutations were identified, indicating that MATR3 (show MATR3 Antibodies) mutations are not a common cause of Amyotrophic lateral sclerosis in Australian familial cases with predominately European ancestry
MATR3 (show MATR3 Antibodies) 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 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.
brain-derived rescue factor p60MONOX
, flavin monooxygenase motif-containing protein of 33 kDa
, flavine monooxygenase motif-containing protein of 33 kDa
, putative monooxygenase p33MONOX
, hypothetical protein LOC100145417
, hypothetical protein LOC100173263