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anti-Human S100A12 Antibodies:
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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
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
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 (show S100A8 Antibodies) and S100A9 (show S100A9 Antibodies) 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 (show S100A8 Antibodies) and S100A9 (show S100A9 Antibodies) may play a role in the pathogenesis of recurrent and chronic OM
Expression of S100A8 (show S100A8 Antibodies), S100A9 (show S100A9 Antibodies) 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 (show AGER Antibodies) has been identified and mapped.
S100A12 functions as a proinflammatory cytokine and activates dermal fibroblasts, causing dermal fibrosis
S100A9 (show S100A9 Antibodies) and S100A12 may have a role in the pathogenesis of pneumonia: S100A9 (show S100A9 Antibodies) and CXCL1 (show CXCL1 Antibodies) may contribute solely in mild pneumonia, and CCL5 (show CCL5 Antibodies) and CXCL11 (show CXCL11 Antibodies) may contribute in severe pneumonia.
These data suggest that S100A12 is part of an innate and adaptive inducible antimicrobial network that contributes to host defense against mycobacteria in infected macrophages
Among the investigated S100-proteins, S100A12 showed the closest association with disease activity and therapeutic response and might therefore provide a valuable biomarker for psoriasis
the expression of S100A12 protein and mRNA was downregulated in a large number of clinical samples of GC. Low expression of S100A12 exhibited a marked propensity toward the clinicopathologic features such as tumor size, depth of invasion, TNM (show ODZ1 Antibodies) stage, Lauren classification, tumor cell differentiation, and poor survival in GC patients.
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