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GLRX3 encodes a member of the glutaredoxin family. Additionally we are shipping Glutaredoxin 3 Antibodies (69) and Glutaredoxin 3 Kits (14) and many more products for this protein.
Showing 10 out of 19 products:
Human GLRX3 Protein expressed in Escherichia coli (E. coli) - ABIN666992
Haunhorst, Berndt, Eitner, Godoy, Lillig: Characterization of the human monothiol glutaredoxin 3 (PICOT) as iron-sulfur protein. in Biochemical and biophysical research communications 2010
Show all 2 references for ABIN666992
findings provide novel insights into the regulation of Grx3, which is crucial for cell survival against environmental insults
These findings provide an advanced view of the functional role of glutaredoxin-3 in iron metabolism.
These in vitro studies suggest that human GLRX3 is important for cytosolic Fe-S protein (show CDSN Proteins) maturation.
Data indicate that silencing of Grx3 in HeLa cells decreases the activities of several cytosolic Fe/S proteins, including iron-regulatory protein 1, a major component of posttranscriptional iron regulation.
these data raise the possibility that the pro-apoptotic role of PICOT is actively regulated via caspase-3 (show CASP3 Proteins)-mediated cleavage.
the unusual [2Fe-2S]-bridging Grx-BolA interaction is conserved in higher eukaryotes and may play a role in signaling cellular iron status in humans.
investigations into role of Grx3: Grx3-knockdown in HeLa cells leads to significant delay in mitotic exit and a higher percentage of binucleated cells.
analysis of primary breast cancer samples demonstrated that enhanced TXNL2 expression correlated with metastasis to the lung and brain and with decreased overall patient survival
Demonstrated a differential expression of PICOT in various cell types, with a predominant cytosolic staining of epithelial cells and low or undetectable levels of PICOT in the stroma.
The present results show a direct correlation between PICOT expression levels and increased cell growth, both in vitro and in vivo.
investigation of role of Grx3: embryos absent Grx3 were small, morphological defects, early embryonic lethality; mRNA ubiquitously expressed in developing embryos, adult tissues; induced during oxidative stress; necessary for cell cycle progression
These data suggest that AM and PICOT might play cooperatively essential roles in embryogenesis as iron-sulfur cluster proteins.
PICOT inhibits cardiac hypertrophy induced by pressure overload; overexpression increased ventricular function and cardiomyocyte contractility measured by ejection fraction & end-systolic pressure of transgenic hearts & peak shortening of cardiomyocytes
PICOT regulated FcepsilonRI (show FCER1A Proteins)-mediated signals in RBL-2H3 cells and acted as a positive regulator on IL-4 (show IL4 Proteins) and TNF-alpha (show TNF Proteins) expression, NFAT (show NFATC1 Proteins) and degranulation and a negative regulator on a JNK (show MAPK8 Proteins) signal pathway.
the precise PICOT protein level significantly affects the process of cardiac hypertrophy and cardiomyocyte contractility.
Data indicate that during embryonic development, depletion of Grx3 severely impairs the maturation of hemoglobin, the major iron-consuming process.
This gene encodes a member of the glutaredoxin family. Glutaredoxins are oxidoreductase enzymes that reduce a variety of substrates using glutathione as a cofactor. The encoded protein binds to and modulates the function of protein kinase C theta. The encoded protein may also inhibit apoptosis and play a role in cellular growth, and the expression of this gene may be a marker for cancer. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 9. Alternatively spliced transcript variants have been observed for this gene.
thioredoxin domain containing 6
, thioredoxin-like 2
, PKC-interacting cousin of thioredoxin
, PKC-theta-interacting protein
, PKCq-interacting protein
, glutaredoxin 4
, thioredoxin-like protein 2
, PKC interacting cousin of thioredoxin