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抗Human S100A12 抗体:
抗Rat (Rattus) S100A12 抗体:
抗Mouse (Murine) S100A12 抗体:
Human Polyclonal S100A12 Primary Antibody for FACS, IHC - ABIN4899193
Ling, Park, Carroll, Nguyen, Lau, Macaubas, Chen, Lee, Sandborg, Milojevic, Kanegaye, Gao, Burns, Schilling, Mellins: Plasma profiles in active systemic juvenile idiopathic arthritis: Biomarkers and biological implications. in Proteomics 2010
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Human Polyclonal S100A12 Primary Antibody for CyTOF, FACS - ABIN4899195
Arumugam, Ramachandran, Gomez, Schmidt, Logsdon: S100P-derived RAGE antagonistic peptide reduces tumor growth and metastasis. in Clinical cancer research : an official journal of the American Association for Cancer Research 2012
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Human Monoclonal S100A12 Primary Antibody for FACS, IHC (fro) - ABIN445906
Roggenbeck, Carew, Charrois, Douglas, Kneteman, Lu, Le, Leslie: Characterization of arsenic hepatobiliary transport using sandwich-cultured human hepatocytes. in Toxicological sciences : an official journal of the Society of Toxicology 2015
S100A12 was a significant predictor of lung alveolar infiltration (OR 2.60, 95%CI 1.35-5.00, p = 0.004). These results suggest that S100A12 has the potential to assess the extent of alveolar infiltration in Pulmonary tuberculosis.
Results indicated that S100A12 could increase the expression of MMP-2 (显示 MMP2 抗体), MMP-9 (显示 MMP9 抗体), and vascular cell adhesion molecule 1 (VCAM-1 (显示 VCAM1 抗体)) in HASMCs via activation of ERK1/2 signal pathway, which leads to injury of HASMCs.
S100A12 binds to CD36 (显示 CD36 抗体) in the low nanomolar range at the CD36 (显示 CD36 抗体) thrombospondin-1 (显示 THBS1 抗体) binding site.
data on the antimicrobial activity of S100A12 have been reported. Proinflammatory role of S100A12 is supported by another newly found receptor, Toll-like receptor 4 (TLR4 (显示 TLR4 抗体)).
Report role of fecal S100A12 assay in the diagnosis and management of inflammatory bowel disease.
The aim of this mini-review was to outline the pleiotropic actions of S100A12 and to highlight the potential clinical importance of this protein in kidney and cardiovascular diseases. [review]
Elevated S100A8 (显示 S100A8 抗体) 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 (显示 S100A8 抗体) and S100A9 (显示 S100A9 抗体) may play a role in the pathogenesis of recurrent and chronic OM
Expression of S100A8 (显示 S100A8 抗体), S100A9 (显示 S100A9 抗体) and S100A12 is modulated by eicosapentaenoic acid and docosahexaenoic acid during Inflammation in adipose tissue and mononuclear cells.
The binding interface between S100A12 and the V domain of RAGE (显示 AGER 抗体) has been identified and mapped.
S100A12 functions as a proinflammatory cytokine and activates dermal fibroblasts, causing dermal fibrosis
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 is proposed to be involved in specific calcium-dependent signal transduction pathways and its regulatory effect on cytoskeletal components may modulate various neutrophil activities.
, S100 calcium-binding protein A12 (calgranulin C)
, calcium-binding protein in amniotic fluid 1
, calgranulin C
, extracellular newly identified RAGE-binding protein
, migration inhibitory factor-related protein 6
, neutrophil S100 protein
, protein S100-A12
, S100 calcium-binding protein A12
, RAGE-binding protein
, cornea-associated antigen