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FAU is the cellular homolog of the fox sequence in the Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV). Zusätzlich bieten wir Ihnen FAU Proteine (18) und FAU Kits (10) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 119 products:
Human Polyclonal FAU Primary Antibody für ELISA, WB - ABIN560851
Glazer, Wang, Yuan, Yin: Musashi1: a stem cell marker no longer in search of a function. in Cell cycle (Georgetown, Tex.) 2008
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Human Polyclonal FAU Primary Antibody für IHC (p), ELISA - ABIN542731
Vladimirov, Ivanov, Karpova, Musolyamov, Egorov, Thiede, Wittmann-Liebold, Otto: Characterization of the human small-ribosomal-subunit proteins by N-terminal and internal sequencing, and mass spectrometry. in European journal of biochemistry / FEBS 1996
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Human Polyclonal FAU Primary Antibody für IHC (p), ELISA - ABIN542733
Kenmochi, Kawaguchi, Rozen, Davis, Goodman, Hudson, Tanaka, Page: A map of 75 human ribosomal protein genes. in Genome research 1998
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Human Polyclonal FAU Primary Antibody für IHC (p), ELISA - ABIN542732
Rossman, Visalli, Komissarova: fau and its ubiquitin-like domain (FUBI) transforms human osteogenic sarcoma (HOS) cells to anchorage-independence. in Oncogene 2003
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Human Monoclonal FAU Primary Antibody für IF, ELISA - ABIN515542
Lee, Johnson, Hallenbeck: Global protein conjugation by ubiquitin-like-modifiers during ischemic stress is regulated by microRNAs and confers robust tolerance to ischemia. in PLoS ONE 2012
FAU knockdown increased the plasma membrane targeting and function of F508del-CFTR, but not of wild-type CFTR. Investigation into the mechanism of action revealed a preferential physical interaction of FAU with mutant CFTR, leading to its degradation.
The FAU rs769440 G allele had higher frequencies in patients with recurrent pregnancy loss.
The C-terminal portion of the encoded protein displays antimicrobial activity against B. megaterium.
In 293T/17 cells, Bcl-G knockdown also attenuates UV-induced apoptosis, so that Bcl-G may constitute a common factor in the pathways by which both FAU and UV-irradiation induce apoptosis
siRNA-mediated downregulation of either Fau or Bcl-G expression inhibited apoptosis, and the inhibition produced by combining the two siRNAs was consistent with control of Bcl-G by Fau.
data support a role for FAU in the regulation of platinum-resistance in ovarian cancer
role in transforming osteogenic sarcoma cells to anchorage-independence
Overexpression of fau in the sense orientation induces cell death, which is inhibited both by Bcl-2 and by inhibition of caspases, in line with its proposed role in apoptosis
the association of MNSFbeta with HSPA8 may promote RANKL-induced osteoclastogenesis.
Collectively, MNSFbeta/FDH complex formation may positively regulate apoptosis in thymocytes.
these results demonstrated that a deficiency in MNSFb is associated with pregnancy loss, probably through reduced P53 and/or increased TNFA production at the fetal-maternal interface.
CD3/CD28-inducible MNSFbeta-Bcl-G complex may be involved in the regulation of T cell function and survival.
MNSFbeta may bind to novel target proteins and negatively regulate TLR-2-mediated signal transduction in macrophages.
these results demonstrate that MNSFbeta/endophilin II inhibits the signal pathway upstream of IKK activation, but not downstream of TLR2 signaling.
The result suggested that the level of MNSFbeta in interimplantation sites was significantly higher as compared with implantation sites in the mouse uterine on Day 4.5 of pregnancy
MNSFbeta cDNA encodes a fusion protein consisting of a ubiquitin-like segment (Ubi-L) and ribosomal protein S30: Ubi-L noncovalently and specifically binds to histone 2A
MNSFbeta might be implicated in the macrophage response to lipopolysaccharide
These results demonstrate that MNSFbeta plays critical roles during the early pregnancy via multiple pathways
post-translational modification of endophilin II by MNSFbeta might be implicated in phagocytosis by macrophages.
This gene is the cellular homolog of the fox sequence in the Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV). It encodes a fusion protein consisting of the ubiquitin-like protein fubi at the N terminus and ribosomal protein S30 at the C terminus. It has been proposed that the fusion protein is post-translationally processed to generate free fubi and free ribosomal protein S30. Fubi is a member of the ubiquitin family, and ribosomal protein S30 belongs to the S30E family of ribosomal proteins. Whereas the function of fubi is currently unknown, ribosomal protein S30 is a component of the 40S subunit of the cytoplasmic ribosome. Pseudogenes derived from this gene are present in the genome. Similar to ribosomal protein S30, ribosomal proteins S27a and L40 are synthesized as fusion proteins with ubiquitin.
40S ribosomal protein S30
, FAU-encoded ubiquitin-like protein
, FBR-MuSV-associated ubiquitously expressed
, Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV) ubiquitously expressed (fox derived)
, monoclonal nonspecific suppressor factor beta
, ribosomal protein S30
, ubiquitin-like protein fubi and ribosomal protein S30
, ubiquitin-like-S30 fusion protein
, Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV) ubiquitously expressed (fox derived); ribosomal protein S30
, ubiquitin-like protein FUBI
, ubiquitin-like/S30 ribosomal fusion protein
, Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV) ubiquitously expressed (fox derived) protein
, Finkel-Biskis-Reilly murine sarcoma virusubiquitously expressed
, Ubiquitin-like protein FUBI
, monoclonal non-specific suppressor factor beta
, monoclonal nonspecific suppressor factor betamonoclonal nonspecific suppressor factor beta
, arsenite-resistance protein