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Human s100b Protein expressed in Escherichia coli (E. coli) - ABIN1097989
Cerofolini, Amato, Borsi, Pagano, Randazzo, Fragai: Probing the interaction of distamycin A with S100β: the "unexpected" ability of S100β to bind to DNA-binding ligands. dans Journal of molecular recognition : JMR 2015
Results showed that our prepared S100B mAbs were suitable for detecting S100B expression in human tissues, furnishing promising tools for further functional investigation and clinical applications.
In this study demonstrated that S100b is elevated in Alzheimer disease cases. and the increased levels in African Americans here may be indicative of increased severity in specific populations.
In neonates, NSE (Montrer ENO2 Protéines) and s100B levels increase after bypass surgery and return below preoperative baseline levels by postoperative day seven. The levels of s100B were positively correlated with circulatory arrest time and negatively correlated with age at time of surgery.
found that S100B plays a crucial role in blocking the interaction site between RAGE (Montrer AGER Protéines) V domain and S100A1 (Montrer S100A1 Protéines). A cell proliferation assay WST (Montrer EEF1A2 Protéines)-1 also supported our results. This report could potentially be useful for new protein development for cancer treatment
the serum levels of S100B protein mediated the association between S100B gene polymorphism and scene selectivity in the retrosplenial cortex
There is a significant correlation between mortality in the critically ill patients in the intensive care unit and increased serum concentration of S100B and NSE (Montrer ENO2 Protéines).
Our findings showed that both S100beta and NSE (Montrer ENO2 Protéines) levels similarly increased during CPB (Montrer CPB1 Protéines) and immediately after CPB (Montrer CPB1 Protéines) during sevoflurane and propofol based anesthesia.
This study demonstrated that S100A12 (Montrer S100A12 Protéines) mRNA levels were significantly decreased in the new cases of untreated MS patients in comparison to healthy controls.
Increased serum levels of S100B protein (and NSE (Montrer ENO2 Protéines)) were observed postoperatively in patients with postoperative cognitive dysfunction.
high S100B expression in Multiple Sclerosis (MS) patient samples suggests its usefulness as a diagnostic biomarker for MS.
Data (including data from studies in knockout mice) suggest that S100b acting as a humoral factor impairs glycolysis in muscle (myoblasts, myotubes, and skeletal muscles) independent of insulin (Montrer INS Protéines) action; this effect appears to be due to inhibition of Gapdh (Montrer GAPDH Protéines) activity from enhanced poly(ADP-ribosyl)ation of Gapdh (Montrer GAPDH Protéines). (S100B = S100 protein, beta polypeptide (Montrer MS4A2 Protéines), neural; Gapdh (Montrer GAPDH Protéines) = glyceraldehyde-3-phosphate dehydrogenase (Montrer GAPDH Protéines))
S100B inhibits C3H/10T1/2 murine embryonic mesenchyma.l cells into osteoblasts. S100B stimulates C3H/10T1/2 cell differentiation into adipocytes.
The results of this study showed that S100B affects behavioral despair in female mice through functional interaction with the 5-HT7 receptor.
Data show that S100B has direct effects on macrophages, enhancing particularly CCL22 (Montrer CCL22 Protéines) and IL-1beta (Montrer IL1B Protéines) expression and modulates the inflammatory response in uveoretinitis and this is likely to be, at least in part, via a direct effect on macrophages.
Data show that high glucose increased protein-protein interaction between Steap4 (Montrer STEAP4 Protéines) and S100B in mesangial (MES13) cells.
high glucoseinduced profibrotic genes (TGFbeta (Montrer TGFB1 Protéines), type IV collagen (Montrer COL4 Protéines) and fibronectin (Montrer FN1 Protéines)) and cell hypertrophyrelated p21WAF1 are dependent on S100B.
S100A1 (Montrer S100A1 Protéines) and S100B are dispensable for endochondral ossification during skeletal development.
Data suggest up-regulation of S100b/RAGE (Montrer AGER Protéines) (advanced glycosylation end-product receptor) signaling plays role in inflammatory interaction between adipocytes/macrophages; adipocyte secretion of S100b is up-regulated by Tnf (tumor necrosis factor-alpha (Montrer TNF Protéines)).
Gioma production of S100B enhancestumor growth through CCL2 (Montrer CCL2 Protéines) upregulation and tumor-associated macrophages chemoattraction.
HMGB1 (Montrer HMGB1 Protéines), S100B, and RAGE (Montrer AGER Protéines) signaling modulate the hippocampal inflammatory response and might play key roles in surgery-induced cognitive decline.
As CSF (Montrer CSF2 Protéines)-S100B levels in calves with neurologic diseases widely differed, the utility of CSF (Montrer CSF2 Protéines)-S100B as a diagnostic marker for neurologic diseases in cattle remains inconclusive.
S100B might participate in the pathophysiology of brain inflammatory disorders via RAGE (Montrer AGER Protéines)-dependent regulation of several inflammation-related events including activation and migration of microglia
X-ray crystallography was used here to characterize an interaction between Ca(2 (Montrer CA2 Protéines))(+)-S100B and TRTK-12, a target that binds to the p53 (Montrer TP53 Protéines)-binding site on S100B.
Intracellular S100B might modulate myoblast differentiation by interfering with MyoD (Montrer MYOD1 Protéines) expression in an NF-kappaB (Montrer NFKB1 Protéines)-dependent manner.
S100b activates guanylate cyclase in a calcium-dependent manner [review]
Structural studies in combination with biochemical data are used to develop a model for calcium-induced activation of human nuclear serine/threonine kinase (NDR (Montrer STK38 Protéines)) kinase by S100B.
S100B shows a sufficient thermostability to resist pasteurization but not spry-drying in milk formulas for preterm and term infants.
Structures of pentamidine (Pnt (Montrer ETS2 Protéines)) bound to Ca(2 (Montrer CA2 Protéines)+)-loaded and Zn(2+),Ca(2 (Montrer CA2 Protéines)+)-loaded S100B were determined by X-ray crystallography at 2.15 A (R(free)=0.266) and 1.85 A (R(free)=0.243) resolution, respectively.
The time course of S100B serum values following spinal cord decompression correlates with outcome; the initial degree of paresis is not a prognostic factor to predict outcome.
This study demonstrated that One singular glomerulus (mdG2) exhibits S100 and parvalbumin (Montrer PVALB Protéines)-positive fibers, apparently originating from all crypt cells plus some microvillous olfactory sensory neuronss.
The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21\; however, this gene is located at 21q22.3. This protein may function in Neurite extension, proliferation of melanoma cells, stimulation of Ca2+ fluxes, inhibition of PKC-mediated phosphorylation, astrocytosis and axonal proliferation, and inhibition of microtubule assembly. Chromosomal rearrangements and altered expression of this gene have been implicated in several neurological, neoplastic, and other types of diseases, including Alzheimer's disease, Down's syndrome, epilepsy, amyotrophic lateral sclerosis, melanoma, and type I diabetes.
S-100 calcium-binding protein, beta chain
, S-100 protein subunit beta
, S100 calcium-binding protein, beta (neural)
, protein S100-B
, S-100 protein beta chain
, S100 calcium-binding protein B
, S100 calcium-binding protein beta (neural)
, S100 protein, beta polypeptide, neural
, S100 protein, beta polypeptide
, S100 calcium binding protein, beta (neural)
, S100 calcium-binding protein, beta
, S-100 calcium-binding protein beta subunit