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HNRNPM belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). Zusätzlich bieten wir Ihnen Heterogeneous Nuclear Ribonucleoprotein M Kits (17) und Heterogeneous Nuclear Ribonucleoprotein M Proteine (6) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 85 products:
Cow (Bovine) Monoclonal HNRNPM Primary Antibody für ICC, IHC (fro) - ABIN152355
Kafasla, Patrinou-Georgoula, Guialis: The 72/74-kDa polypeptides of the 70-110 S large heterogeneous nuclear ribonucleoprotein complex (LH-nRNP) represent a discrete subset of the hnRNP M protein family. in The Biochemical journal 2001
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Cow (Bovine) Monoclonal HNRNPM Primary Antibody für ICC, IF - ABIN152356
Vautier, Chesné, Cunha, Calado, Renard, Carmo-Fonseca: Transcription-dependent nucleocytoplasmic distribution of hnRNP A1 protein in early mouse embryos. in Journal of cell science 2001
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Cow (Bovine) Polyclonal HNRNPM Primary Antibody für WB - ABIN2778962
Ewing, Chu, Elisma, Li, Taylor, Climie, McBroom-Cerajewski, Robinson, OConnor, Li, Taylor, Dharsee, Ho, Heilbut, Moore, Zhang, Ornatsky, Bukhman, Ethier, Sheng, Vasilescu, Abu-Farha, Lambert, Duewel et al.: Large-scale mapping of human protein-protein interactions by mass spectrometry. ... in Molecular systems biology 2007
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Human Polyclonal HNRNPM Primary Antibody für ELISA, WB - ABIN561915
Venables, Koh, Froehlich, Lapointe, Couture, Inkel, Bramard, Paquet, Watier, Durand, Lucier, Gervais-Bird, Tremblay, Prinos, Klinck, Elela, Chabot: Multiple and specific mRNA processing targets for the major human hnRNP proteins. in Molecular and cellular biology 2008
Human Monoclonal HNRNPM Primary Antibody für IF, IHC (p) - ABIN518184
Jeon, Jeong, Baek, Koo, Park, Yang, Yu, Kim, Pak: Network clustering revealed the systemic alterations of mitochondrial protein expression. in PLoS computational biology 2011
suggesting that Rump and Lost are part of a core localization complex that promotes utilization of the late localization pathway by multiple mRNAs in parallel
Data show that depletion of Hrp59 by RNA interference reduces the levels of Rrp4 at transcription sites, which suggests that Hrp59 is needed for the exosome to stably interact with nascent pre-mRNPs.
Hrp59 is required for the expression of target mRNAs. Hrp59 binds preferentially to exonic splicing enhancers and our results provide new insights into the role of hnRNP M in splicing regulation.
the ability of HRP59 to regulate the alternative splicing of its own pre-mRNA serves in a negative feedback loop that controls the levels of the HRP59 protein and maintains the homeostasis of the splicing environment.
Rumpelstiltskin (rump) regulates anterior-posterior axis patterning by functioning as a direct-acting nanos mRNA localization factor.
Overexpression of hnRNPM promotes breast cancer aggressiveness by regulating the level of CD44s and indicates a poor prognosis.
Data suggest that both heterogeneous nuclear ribonucleoprotein (zeige PCBP2 Antikörper) type M (HNRPM) and solute carrier (zeige SERTAD2 Antikörper) 1A5 (SLC1A5 (zeige SLC1A5 Antikörper)) have role in the pathogenesis of ovarian cancer.
p54nrb and hnRNPM knockdown silences the FGF1 promoter-dependent accumulation of mRNA during myoblast differentiation.
Results suggest that glyceraldehyde-modified hnRNPM alters gene expression in nonalcoholic fatty liver disease.
The authors propose that cleavage of and subverting the function of hnRNPM by 3C protease is a general strategy utilized by picornaviruses to facilitate viral infection.
our data suggest that TAF15 (zeige TAF15 Antikörper) and TLS/FUS (zeige FUS Antikörper) operate within similar but not identical hnRNP M-TET protein complexes to influence the transcriptional or post-transcriptional output of a particular cell type.
findings demonstrate a novel molecular mechanism through which tumor metastasis is endowed by the hnRNPM-mediated splicing program.
Our results provide a clue that hnRNP M is a potential therapeutic target for Spinal muscular atrophy
The present data demonstrate that the upregulation of HnRNP M is involved in human colorectal epithelial carcinogenesis and may serve as a carcinoma biomarker for colorectal cancer.
Mechanistic control of carcinoembryonic antigen-related cell adhesion molecule-1 (CEACAM1 (zeige CEACAM1 Antikörper)) splice isoforms by the heterogeneous nuclear ribonuclear proteins hnRNP L (zeige HNRNPL Antikörper), hnRNP A1 (zeige HNRNPA1 Antikörper), and hnRNP M.
identify Nova-1 (zeige NOVA1 Antikörper) and hnRNP M as D2R (zeige DRD2 Antikörper) pre-mRNA-binding proteins and show their antagonistic role in the alternative splicing of D2R (zeige DRD2 Antikörper) pre-mRNA.
This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has three repeats of quasi-RRM domains that bind to RNAs. This protein also constitutes a monomer of the N-acetylglucosamine-specific receptor which is postulated to trigger selective recycling of immature GlcNAc-bearing thyroglobulin molecules. Alternative splicing results in multiple transcript variants.
heterogeneous nuclear ribonucleoprotein M
, Heterogeneous nuclear ribonucleoprotein M
, heterogeneous nuclear ribonucleoprotein M-like
, CEA receptor
, N-acetylglucosamine receptor 1
, heterogenous nuclear ribonucleoprotein M4
, hnRNA-binding protein M4
, hnRNP M
, M4 protein