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anti-Human HMGB1 Anticorps:
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Human Monoclonal HMGB1 Primary Antibody pour CyTOF, FACS - ABIN4899428
Liou, Adler, Keogh, Li, Jensen, Walsh, Packer, Clark, Carveth, Chen, Rogers, Lane, Moore, Sturrock, Paine, Cox, Hoidal: Sputum biomarkers and the prediction of clinical outcomes in patients with cystic fibrosis. dans PLoS ONE 2012
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Cow (Bovine) Polyclonal HMGB1 Primary Antibody pour ELISA, FACS - ABIN250703
Barlan, Griffin, McGuire, Wiethoff: Adenovirus membrane penetration activates the NLRP3 inflammasome. dans Journal of virology 2010
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Human Polyclonal HMGB1 Primary Antibody pour IF (p), IHC (p) - ABIN671616
Zhao, Hu, Sun, Sun: The high mobility group box 1 protein of Sciaenops ocellatus is a secreted cytokine that stimulates macrophage activation. dans Developmental and comparative immunology 2011
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Human Monoclonal HMGB1 Primary Antibody pour IF, IHC (p) - ABIN561281
Krüger, Krick, Dhillon, Lerner, Ames, Bromberg, Lin, Walsh, Vella, Fischereder, Krämer, Colvin, Heeger, Murphy, Schröppel: Donor Toll-like receptor 4 contributes to ischemia and reperfusion injury following human kidney transplantation. dans Proceedings of the National Academy of Sciences of the United States of America 2009
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Human Monoclonal HMGB1 Primary Antibody pour IF, IHC (p) - ABIN561282
Franciosi, Govorukhina, Fusetti, Poolman, Lodewijk, Timens, Postma, ten Hacken, Bischoff: Proteomic analysis of human epithelial lining fluid by microfluidics-based nanoLC-MS/MS: a feasibility study. dans Electrophoresis 2013
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Human Monoclonal HMGB1 Primary Antibody pour IF, IHC (p) - ABIN1326935
Kim, Ku, Bae: Persicarin is anti-inflammatory mediator against HMGB1-induced inflammatory responses in HUVECs and in CLP-induced sepsis mice. dans Journal of cellular physiology 2013
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Human Monoclonal HMGB1 Primary Antibody pour IF, IHC (p) - ABIN561286
Zhou, Huang, Poon, Chen, Chan, Ng, Guan, Watt, Lu, Yuen, Zheng: Functional dissection of an IFN-alpha/beta receptor 1 promoter variant that confers higher risk to chronic hepatitis B virus infection. dans Journal of hepatology 2009
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Human Monoclonal HMGB1 Primary Antibody pour FACS - ABIN4896097
Rath, Geisler, Gawaz, Vogel: HMGB1 Expression Level in Circulating Platelets is not Significantly Associated with Outcomes in Symptomatic Coronary Artery Disease. dans Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2017
Human Monoclonal HMGB1 Primary Antibody pour FACS - ABIN4896098
Mobarrez, Antoniewicz, Bosson, Kuhl, Pisetsky, Lundbäck: The effects of smoking on levels of endothelial progenitor cells and microparticles in the blood of healthy volunteers. dans PLoS ONE 2014
Hamster Monoclonal HMGB1 Primary Antibody pour FACS, IF - ABIN2474000
Lange, Vasquez: HMGB1: the jack-of-all-trades protein is a master DNA repair mechanic. dans Molecular carcinogenesis 2009
HMGB1 silencing promoted the susceptibility of retinoblastoma cells to chemotherapeutic drugs through downregulating NF-kappaB (Montrer NFKB1 Anticorps).
HMGB1 possesses beneficial actions, such as endothelial activation, enhancement of neurite outgrowth, and neuronal survival in ischemic stroke. [review]
HMGB1 mediates fibroblast activity via RAGE (Montrer AGER Anticorps)-MAPK (Montrer MAPK1 Anticorps) and NF-kappaB (Montrer NFKB1 Anticorps) signaling in keloid scar formation.
Serum HMGB1 may be a potential marker to monitor the surgical course in patients undergoing surgery for colorectal cancer.
the promotive effects of HuR (Montrer ELAVL1 Anticorps) overexpression on the inflammatory response were attenuated when HUVECs were cotreated with HMGB1 short hairpin RNA. Therefore, the present results indicated that the ectopic expression of HuR (Montrer ELAVL1 Anticorps) may induce inflammatory responses and thus sepsis by activating the HMGB1 signaling pathway.
This is the first report to examine the risk factors associated with HMGB1 SNPs in the development of Rheumatoid arthritis disease in the Chinese Han population.
HMGB1/IL-1beta (Montrer IL1B Anticorps) complexes released after burn injuries can modulate immune responses
The HMGB1 may also be involved in mediating early stress responses in Spiral ganglion neurons(SGNs). They found that HMGB1 and p-c-Jun (Montrer JUN Anticorps) (an activated form of an early stress-activated transcription factor) accumulated in the nuclei of the SGNs.
hypoxia affects tumour growth and metastasis in melanoma and depict HMGB1 as a potential therapeutic target.
Our study suggests that HMGB1 CSF (Montrer CSF2 Anticorps) levels are increased in patients with anti-NMDAR (Montrer GRIN1 Anticorps) encephalitis
these results suggest that miR1423p functions as a negative regulator of neuropathic pain development through the downregulation of HMGB1, indicating that miR1423p may serve as a potential therapeutic target for neuropathic pain
Chronic unpredictable stress (CUS) promotes significant morphological changes and causes robust upregulation of HMGB1 messenger RNA in enriched hippocampal microglia and robust and persistent upregulation of RAGE (Montrer AGER Anticorps) messenger RNA. CUS increased surface expression of RAGE (Montrer AGER Anticorps) protein on hippocampal microglia and anhedonic behavior. HMGB1 infusion into the hippocampus was sufficient to cause anhedonic behavior.
Chloroquine improves the response to ischemic muscle injury and increases HMGB1 after arterial ligation.
Data suggest high mobility group box 1 (HMGB1) expression may be associated with the protective effect of saquinavir (SQV).
Study shows that the disulfide form of high mobility group box-1 mediates bladder pain directly (not secondary to inflammation or injury) through activation of toll-like receptor 4 (Montrer TLR4 Anticorps) receptors in the bladder.
findings suggest that HMGB1 induces the transcytosis of albumin (Montrer ALB Anticorps) via RAGE (Montrer AGER Anticorps)-dependent Src (Montrer SRC Anticorps) phosphorylation and Cav-1 (Montrer CAV1 Anticorps) phosphorylation. These studies revealed a new mechanism of HMGB1-induced endothelial hyperpermeability.
The injury resistance in the setting of liver fibrosis is accompanied by the inhibition of HMGB1 translocation and release as well as the suppression of HMGB1-related proinflammatory immune responses.
These data demonstrate that 2% H2 inhalation may be a promising therapeutic strategy for intestinal injuries caused by severe sepsis through the regulation of HO-1 (Montrer HMOX1 Anticorps) and HMGB1 release. In addition, Nrf2 (Montrer NFE2L2 Anticorps) plays a key role in the protective effects of H2 against intestinal damage in this disease.
HMGB1 can act as an adjuvant in modulating the bovine immune system and thus lays a foundation for using HMGB1 as an adjuvant in various bovine vaccine preparations.
Single-nucleotide polymorphism in the 3'-untranslated region of the HMGB1 gene affects the binding of target bta-miR (Montrer MYLIP Anticorps)-223 and is involved in mastitis.
The mechanisms of interaction of the non-histone chromosomal protein (Montrer HMGB2 Anticorps) HMGB1 and linker histone H1 (Montrer H1F0 Anticorps) with DNA have been studied using circular dichroism and absorption spectroscopy.
HMGB1 is able to induce considerable changes in DNA structure upon binding even when the amount of the protein directly associated with DNA is low
Interaction between non-histone chromatin protein HMGB1 and linker histone H1 (Montrer H1F0 Anticorps)
HMGB-1 might play a role in the pathological thickening of subchondral bone plate/osteophyte formation.
Analysis of mechanical response generated by binding of DNA-bending protein HMGB1 to single tethered 48.5 kb lambda-DNA molecules finds that compaction of DNA increases with increasing HMGB1 concentration.
Thrombomoduln not only binds to HMGB1 but also aids the proteolytic cleavage of HMGB1 by thrombin (Montrer F2 Anticorps).
SCARA5 (Montrer SCARA5 Anticorps) is an HMGB1 recognition receptor that is negatively involved in HMGB1-mediated inflammation in pufferfish (Tetraodon nigroviridis) and zebrafish (Danio rerio) models.
HMGB1 is a critical factor for brain development, enabling survival and proliferation of neural progenitors that will form the forebrain structures.
Systemic HMGB-1 levels were significantly elevated in both trauma groups when compared to the sham group. Haemorrhagic shock severity and duration were positively correlated with HMGB-1 levels and compared to baseline values, concentrations remained significantly increased in severe hemorrhage when compared to moderate hemorrhage.
high levels of HMGB1 in the small intestine and its relation to high levels of HMGB1 in plasma of piglets infected with E. coli O55 that suffered from infection correlated with high levels of inflammatory cytokines and bacterial translocation; levels were higher than HMGB1 levels in piglets with mild clinical symptoms
HMGB-1 may participate in the inflammatory response and liver injury in the late stage of acute liver failure
High mobility group box-1 and nucleosomes might have use as biomarkers for horses with gastrointestinal disease.
Extracellular HMGB-1 is widespread only in synovial membrane from diseased joints in horses with osteoarthritis.
Osteochondral injury was associated with a significant increase in synovial HMGB-1 concentrations in horses with joint injuries, compared with results for clinically normal horses.
Airway pressure release ventilation reduces bronchoalveolar lavage fluid HMGB1 levels and lung water, preserving oxygenation and systemic blood pressure in experimental acute respiratory distress syndrome.
heparin binding protein that facilitates neurite outgrowth
, Sulfoglucuronyl carbohydrate binding protein
, high mobility group protein 1
, high mobility group protein B1
, high-mobility group (nonhistone chromosomal) protein 1
, high-mobility group box 1
, sulfoglucuronyl carbohydrate binding protein
, high mobility group box 1
, high mobility group 1 protein
, high mobility group protein HMG1
, non-histone protein HMG1
, high mobility group protein B1-like protein
, High mobility group protein B1
, high mobility group protein B1-like
, High mobility group protein 1
, heparin-binding protein p30
, high mobility group 1