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抗Human S100A8 抗体:
抗Rat (Rattus) S100A8 抗体:
抗Mouse (Murine) S100A8 抗体:
Human Monoclonal S100A8 Primary Antibody for EIA, IHC (fro) - ABIN111891
Odink, Cerletti, Brüggen, Clerc, Tarcsay, Zwadlo, Gerhards, Schlegel, Sorg: Two calcium-binding proteins in infiltrate macrophages of rheumatoid arthritis. in Nature 1987
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Human Monoclonal S100A8 Primary Antibody for EIA, IHC (fro) - ABIN111890
Brandtzaeg, Jones, Flavell, Fagerhol: Mac 387 antibody and detection of formalin resistant myelomonocytic L1 antigen. in Journal of clinical pathology 1989
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Mouse (Murine) Polyclonal S100A8 Primary Antibody for IF (p), IHC (p) - ABIN749273
Nguyen, Fentress, Qiu, Yun, Cox, Chawla: Circadian gene Bmal1 regulates diurnal oscillations of Ly6C(hi) inflammatory monocytes. in Science (New York, N.Y.) 2013
Human Monoclonal S100A8 Primary Antibody for IA, FACS - ABIN2192036
Robinson, Tessier, Poulsom, Hogg: The S100 family heterodimer, MRP-8/14, binds with high affinity to heparin and heparan sulfate glycosaminoglycans on endothelial cells. in The Journal of biological chemistry 2002
Human Polyclonal S100A8 Primary Antibody for ELISA, WB - ABIN4242803
Eggers, Sikora, Lorenz, Taubert, Moobed, Baumann, Stangl, Stangl: RAGE-dependent regulation of calcium-binding proteins S100A8 and S100A9 in human THP-1. in Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2011
Human Polyclonal S100A8 Primary Antibody for IHC, IHC (p) - ABIN4351730
Ellis, LaRocque, Uddin, Krastins, Mayo-Smith, Sarracino, Karlsson, Rahman, Shirin, Bhuiyan, Chowdhury, Khan, Ryan, Calderwood, Qadri, Harris: Comparative proteomic analysis reveals activation of mucosal innate immune signaling pathways during cholera. in Infection and immunity 2015
S100A8 methylation has a role in diagnosis and prognosis of hepatocellular carcinoma
This study demonstrated that S100A8 was detected in the serums of Alzheimer disease patients
Studies indicate S100A8 as the most overexpressed gene, and the cell cycle pathway as the most promising biomarker and therapeutic target for relapsed childhood B-acute lymphoblastic leukemia (B-ALL).
Low S100A8 expression is associated with head and neck neoplasms.
Report role of fecal calprotectin assay in the diagnosis and management of inflammatory bowel disease.
S100A8 and S100A9 (显示 S100A9 抗体) aggravate Coxsackievirus B3-induced myocarditis and might serve as therapeutic targets in inflammatory cardiomyopathies.
Data suggest that fecal calprotectin may be a potential biomarker to identify patients with ankylosing spondylitis (AS) at risk of developing inflammatory bowel disease (IBD).
Elevated S100A8 and S100A9 (显示 S100A9 抗体) gene expression in SP-infected HMEECs and in the middle ear mucosa of OM, minor co-localized with neutrophil markers suggests that middle ear epithelial cell secretion of S100A8 and S100A9 (显示 S100A9 抗体) may play a role in the pathogenesis of recurrent and chronic OM
results of this study support an additional role of calprotectin in assessing inflammatory activity in patients with RA
Data show that E3 ubiquitin ligase (显示 MUL1 抗体) HRD1 (HRD1 (显示 SYVN1 抗体)) decreased the protein level of S100A8 through ubiquitination.
Data suggest that up-regulation of S100A8 and S100A9 (显示 S100A9 抗体) is a key component of early endometrial response to uterine involution in the post-partum period and to prevent chronic endometritis/uterine inflammation; up-regulation can be influenced by diet.
Study verified porcine calprotectin (S100A8/A9) expression at the protein level in multiple Haemophilus parasuis infected tissues and explored their molecular characterization.
data suggest that S100A8/A9 acts directly on BV-2 microglial cells via binding to TLR4 (显示 TLR4 抗体) and RAGE (显示 AGER 抗体) on the membrane and then stimulates the secretion of proinflammatory cytokines through ERK (显示 EPHB2 抗体) and JNK (显示 MAPK8 抗体)-mediated NF-kappaB (显示 NFKB1 抗体) activity in BV-2 microglial cells.
The results obtained in the present study demonstrate for the first time that S100A8 as well as MyD88 (显示 MYD88 抗体) and NF-B are activated by T3 and that these molecules are directly involved in the thyroid hormone (显示 PTH 抗体)-induced cardiac hypertrophic response. These data suggest that one of the mechanisms underlying T3-dependent cardiac hypertrophy/failure may involve the activation of an inflammatory pathway.
Like S100A8, S100A9 (显示 S100A9 抗体) and S100A8/A9 reduced neutrophil influx in acute lung injury provoked by lipopolysaccharide (LPS (显示 TLR4 抗体)) challenge.
theses findings reveal unexpected gene expression differences between WT and KO mice at a young age (in the absence of physiological stress), and address the hypothesis that Mrp8 and Mrp14 (显示 S100A9 抗体) accumulation promotes age-related inflammation
Neutrophil-derived S100A8/A9 promotes thrombocytosis in diabetic mice
Perinatal alarmins S100A8 and S100A9 (显示 S100A9 抗体) specifically altered MyD88 (显示 MYD88 抗体)-dependent proinflammatory gene programs. S100 programming prevented hyperinflammatory responses without impairing pathogen defense. TRIF (显示 RNF138 抗体)-adaptor-dependent regulatory genes remained unaffected by perinatal S100 programming and responded strongly to lipopolysaccharide, but were barely expressed.
S100a8 upregulation triggers NF-kappaB (显示 NFKB1 抗体) signal pathway through RAGE (显示 AGER 抗体) and TLR4 (显示 TLR4 抗体), in response to laser-induced dermis wound healing.
Although MRP-8/-14 expression is highly increased in experimental, these proteins do not contribute to the pathogenesis in the effector phase of epidermolysis bullosa acquisita and bullous pemphigoid (显示 DST 抗体).
TLR4 (显示 TLR4 抗体), TLR2 also contributed to Mrp8-induced inflammatory response and tolerance.
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. This protein may function in the inhibition of casein kinase and as a cytokine. Altered expression of this protein is associated with the disease cystic fibrosis.
, S100 calcium-binding protein A8 (calgranulin A)
, calgranulin A
, calprotectin L1L subunit
, cystic fibrosis antigen
, leukocyte L1 complex light chain
, migration inhibitory factor-related protein 8
, protein S100-A8
, urinary stone protein band A
, S100 calcium binding protein A8 (calgranulin A)
, S100 calcium binding protein A8
, S100 calcium-binding protein A8
, neutrophil cytosolic 7 kDa protein
, chemotactic S100 protein
, chemotactic cytokine CP-10
, pro-inflammatory S100 cytokine
, macrophage migration inhibitory factor-related protein-8