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anti-Human MMP4 Antikörper:
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Human Monoclonal MMP4 Primary Antibody für IF, WB - ABIN968762
Buaas, Lee, Edelhoff, Disteche, Braun: Cloning and characterization of the mouse interleukin enhancer binding factor 3 (Ilf3) homolog in a screen for RNA binding proteins. in Mammalian genome : official journal of the International Mammalian Genome Society 1999
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Human Monoclonal MMP4 Primary Antibody für IF, WB - ABIN968761
Patel, Vestal, Xu, Bandyopadhyay, Guo, Erme, Williams, Sen: DRBP76, a double-stranded RNA-binding nuclear protein, is phosphorylated by the interferon-induced protein kinase, PKR. in The Journal of biological chemistry 1999
Show all 4 Pubmed References
Data support a model in which NF45 (zeige ILF2 Antikörper), NF90, and NF110 operate in feedback loops that enable them, through both overlapping and independent targets, to help balance the push and pull of pluripotency and differentiation cues.
Reduction in the expression of YBX1 (zeige YBX1 Antikörper) and ILF3 controls the expression of pluripotency-related genes in ESCs (zeige NR2E3 Antikörper), suggesting their roles in further regulation of the pluripotent state of ESCs (zeige NR2E3 Antikörper).
NF90-NF45 (zeige ILF2 Antikörper) complex induces centronuclear myopathy through increased dynamin 2 (zeige DNM2 Antikörper) expression by an NF90-NF45 (zeige ILF2 Antikörper)-induced reduction of miR (zeige MLXIP Antikörper)-133a expression in vivo.
This work allows to establish a link between Ilf3 and NF90 functions, as RNA binding proteins, and their interacting partners implicated in these functions.
High expression of nuclear factor 90 leads to mitochondrial degradation in skeletal and cardiac muscles through a negative regulation of ribosomes via interaction with ribosomal factors.
cloning of human NF90
characterization of NFAR-1 and NFAR-2 splice forms in human sample
NF90 regulates cell cycle exit and terminal myogenic differentiation by direct binding to the 3'-untranslated region of MyoD (zeige MYOD1 Antikörper) and p21WAF1/CIP1 mRNAs
ADAR1 (zeige ADAR Antikörper) has the potential both to change information content through editing of mRNA and to regulate gene expression through interacting with NF90
NF90 regulates inducible IL-2 (zeige IL2 Antikörper) gene expression in T cells.
Studies suggest a two-component model for the binding of CBTF with gata2 (zeige GATA2 Antikörper) promoter, requiring both a CCAAT and A-form DNA, and the double stranded RNA binding domains (dsRBDs) of CBTF component Xilf3 must be active for both binding to the promoter.
Reprot a coordinated regulation of circRNA biogenesis and function by NF90/NF110 in viral infection.
The NF90 regulates PARP1 (zeige PARP1 Antikörper) mRNA stability in hepatocellular carcinoma cells, and NF90 is a potential target to inhibit PARP1 (zeige PARP1 Antikörper) activity.
Variants in ILF3 gene is associated with thrombosis.
these data establish miR (zeige MLXIP Antikörper)-590-5p as an anti-onco-miR (zeige MLXIP Antikörper) that inhibits colorectal cancer angiogenesis and metastasis through a new mechanism involving NF90/VEGFA (zeige VEGFA Antikörper) signaling axis.
The data suggest that features of both the N- and C-termini of NF90 participate in the heterodimerization with NF45 (zeige ILF2 Antikörper) and that the formation of NF90-NF45 (zeige ILF2 Antikörper) changes the conformation of NF90's RNA-binding motifs to a status in which the co-operative interplay of the RNA-binding motifs is optimal.
NF90-NF45 (zeige ILF2 Antikörper) stimulates an elevation of EGF receptor (zeige EGFR Antikörper) levels via the suppression of miR-7 (zeige LILRB1 Antikörper) biogenesis, resulting in the promotion of cell proliferation in Hepatocellular Carcinoma.
NF90 exerts its antiviral activity by antagonizing the inhibitory role of NS1 (zeige PTPN11 Antikörper) on PKR (zeige PKLR Antikörper) phosphorylation
Deletion of the RNA binding domains of NF45 (zeige ILF2 Antikörper) and NF90 diminished the enhancement of HIV infection and gene expression.
These data suggest that, like ADAR2 (zeige ADARB1 Antikörper), underlying sequences in dsRNA may influence how NF90 recognizes its target RNAs
The NF90 C-terminus is involved in conformational changes in the protein after RNA binding.
This gene encodes a double-stranded RNA (dsRNA) binding protein that complexes with other proteins, dsRNAs, small noncoding RNAs, and mRNAs to regulate gene expression and stabilize mRNAs. This protein was first discovered to be a subunit of the nuclear factor of activated T-cells (NFAT)\; a transcription factor required for T-cell expression of interleukin 2. NFAT is a heterodimer of 45 kDa and 90 kDa proteins, the larger of which is the product of this gene. These proteins have been shown to affect the redistribution of nuclear mRNA to the cytoplasm. Knockdown of NF45 or NF90 protein retards cell growth\; possibly by inhibition of mRNA stabilization. In contrast, an isoform (NF110) of this gene that is predominantly restricted to the nucleus has only minor effects on cell growth when its levels are reduced. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
M phase phosphoprotein 4
, interleukin enhancer-binding factor 3
, nuclear factor 90
, nuclear factor associated with dsRNA
, CCAAT box transcription factor p122 subunit
, CCAAT box transcription factor subunit
, Double-stranded RNA-binding protein 4F.1
, dsRNA-binding protein 4F.1
, interleukin enhancer-binding factor 3-A
, M-phase phosphoprotein 4
, double-stranded RNA-binding protein, 76 kD
, dsRNA binding protein NFAR-2/MPP4
, nuclear factor of activated T-cells 90 kDa
, nuclear factor of activated T-cells, 90 kD
, translational control protein 80
, interleukin enhancer binding factor 3, 90kDa
, interleukin enhancer-binding factor 3 homolog