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Human S100A8 ELISA Kit für Sandwich ELISA - ABIN414827
Nair, Khanna, Singh: Association of Increased S100A8 Serum Protein with Early Pregnancy Loss. in American journal of reproductive immunology (New York, N.Y. : 1989) 2015
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Human S100A8 ELISA Kit für Sandwich ELISA - ABIN2685413
Xu, Yen, Geczy: Il-10 up-regulates macrophage expression of the S100 protein S100A8. in Journal of immunology (Baltimore, Md. : 1950) 2001
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Mouse (Murine) S100A8 ELISA Kit für Sandwich ELISA - ABIN425109
Sekimoto, Kishida, Nakatsuji, Nakagawa, Funahashi, Shimomura: High circulating levels of S100A8/A9 complex (calprotectin) in male Japanese with abdominal adiposity and dysregulated expression of S100A8 and S100A9 in adipose tissues of obese mice. in Biochemical and biophysical research communications 2012
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Human S100A8 ELISA Kit für Sandwich ELISA - ABIN365760
Obry, Lequerré, Hardouin, Boyer, Fardellone, Philippe, Le Loët, Cosette, Vittecoq: Identification of S100A9 as Biomarker of Responsiveness to the Methotrexate/Etanercept Combination in Rheumatoid Arthritis Using a Proteomic Approach. in PLoS ONE 2014
Mouse (Murine) S100A8 ELISA Kit für Sandwich ELISA - ABIN822167
Repasy, Martinez, Lee, West, Li, Kornfeld: Bacillary replication and macrophage necrosis are determinants of neutrophil recruitment in tuberculosis. in Microbes and infection / Institut Pasteur 2015
Report role of fecal calprotectin assay in the diagnosis and management of inflammatory bowel disease.
S100A8 and S100A9 (zeige S100A9 ELISA Kits) 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 (zeige S100A9 ELISA Kits) 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 (zeige S100A9 ELISA Kits) 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 HRD1 (HRD1 (zeige SYVN1 ELISA Kits)) decreased the protein level of S100A8 through ubiquitination.
High S100A8 expression is associated with glioblastoma.
This study implicates S100A8 and S100A9 (zeige S100A9 ELISA Kits) as important mediators of tumor cell aggressiveness, and highlights the therapeutic potential of S100A8 and S100A9 (zeige S100A9 ELISA Kits) for interference of metastasis.
Data indicate a statistical correlation between fecal calprotectin (FC) and gastrointestinal graft-versus-host disease (GvHD).
Perinatal alarmins S100A8 and S100A9 (zeige S100A9 ELISA Kits) specifically altered MyD88 (zeige MYD88 ELISA Kits)-dependent proinflammatory gene programs. S100 programming prevented hyperinflammatory responses without impairing pathogen defense. TRIF (zeige TRIM69 ELISA Kits)-adaptor-dependent regulatory genes remained unaffected by perinatal S100 programming and responded strongly to lipopolysaccharide, but were barely expressed.
Data suggest that up-regulation of S100A8 and S100A9 (zeige S100A9 ELISA Kits) 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.
Neutrophil-derived S100A8/A9 promotes thrombocytosis in diabetic mice
Perinatal alarmins S100A8 and S100A9 (zeige S100A9 ELISA Kits) specifically altered MyD88 (zeige MYD88 ELISA Kits)-dependent proinflammatory gene programs. S100 programming prevented hyperinflammatory responses without impairing pathogen defense. TRIF (zeige RNF138 ELISA Kits)-adaptor-dependent regulatory genes remained unaffected by perinatal S100 programming and responded strongly to lipopolysaccharide, but were barely expressed.
S100a8 upregulation triggers NF-kappaB (zeige NFKB1 ELISA Kits) signal pathway through RAGE (zeige AGER ELISA Kits) and TLR4 (zeige TLR4 ELISA Kits), 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 (zeige DST ELISA Kits).
TLR4 (zeige TLR4 ELISA Kits), TLR2 (zeige TLR2 ELISA Kits) also contributed to Mrp8-induced inflammatory response and tolerance.
S100A8 appears to play a crucial role in the activation of the TLR4 (zeige TLR4 ELISA Kits)/MD-2 (zeige LY96 ELISA Kits) pathway and the promotion of a tumor growth-enhancing immune microenvironment.
Rps14 (zeige RPS14 ELISA Kits) haploinsufficiency in del(5q) myelodysplastic syndrome is linked to activation of the innate immune system and induction of S100A8-S100A9 (zeige S100A9 ELISA Kits) expression, leading to a p53 (zeige TP53 ELISA Kits)-dependent erythroid differentiation defect.
S100A8 is primarily produced from CXCR2 (zeige CXCR2 ELISA Kits)-expressing CD11b (zeige ITGAM ELISA Kits)(+)Gr-1 (zeige GSR ELISA Kits)(high) cells, and it upregulates TNF-alpha (zeige TNF ELISA Kits) production in CD11b (zeige ITGAM ELISA Kits)(+)F4/80(+) cells through cellular cross-talk, which is an important mechanism in the development of Nonalcoholic fatty liver disease
Alarmins S100A8/S100A9 (zeige S100A9 ELISA Kits) aggravate osteophyte formation in experimental osteoarthritis and predict osteophyte progression in early human symptomatic osteoarthritis.
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