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The protein encoded by S100A4 is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. Additionally we are shipping s100a4 Proteins (38) and s100a4 Kits (26) and many more products for this protein.
Showing 10 out of 235 products:
Human Monoclonal s100a4 Primary Antibody for IF, WB - ABIN395081
van Dieck, Lum, Teufel, Fersht: S100 proteins interact with the N-terminal domain of MDM2. in FEBS letters 2010
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Human Polyclonal s100a4 Primary Antibody for IHC (p), IHC - ABIN188680
Jiang, Xu, Mao, Li, Fang, Zhou, Liu, He, Zhao, Yang, Dai: Rheb/mTORC1 signaling promotes kidney fibroblast activation and fibrosis. in Journal of the American Society of Nephrology : JASN 2013
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Human Polyclonal s100a4 Primary Antibody for IHC, IHC (p) - ABIN4351669
Laguë, Detmar, Paquet, Boyer, Richards, Adamson, Boerboom: Decidual PTEN expression is required for trophoblast invasion in the mouse. in American journal of physiology. Endocrinology and metabolism 2010
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Mouse (Murine) Polyclonal s100a4 Primary Antibody for IHC (p), WB - ABIN655727
Miranda, Loeser, Yammani: Sumoylation and nuclear translocation of S100A4 regulate IL-1beta-mediated production of matrix metalloproteinase-13. in The Journal of biological chemistry 2010
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Human Polyclonal s100a4 Primary Antibody for IHC, ELISA - ABIN334485
Li, Bresnick: The S100A4 metastasis factor regulates cellular motility via a direct interaction with myosin-IIA. in Cancer research 2006
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Cat (Feline) Polyclonal s100a4 Primary Antibody for IHC (p) - ABIN181369
Schäfer, Heizmann: The S100 family of EF-hand calcium-binding proteins: functions and pathology. in Trends in biochemical sciences 1996
Show all 2 references for ABIN181369
Human Polyclonal s100a4 Primary Antibody for IHC (p) - ABIN181370
Ilg, Schäfer, Heizmann: Expression pattern of S100 calcium-binding proteins in human tumors. in International journal of cancer. Journal international du cancer 1996
Show all 2 references for ABIN181370
Cell invasion (matrigel) was reduced only in the Hs578T cells (p < 0.01). Silencing decreased the expression of the prometastatic molecules S100A4 and TGFbetaR2 in both cell lines and CD44 (show CD44 Antibodies) in Hs578T cells .We conclude that ECM1 (show ECM1 Antibodies) is a key player in the metastatic process and regulates the actin cytoskeletal architecture of aggressive breast cancer cells at least in part via alterations in S100A4 and Rho A (show RHOA Antibodies).
Aberrant S100A4 expression may predictendometrial cancer (EC) progression and play an important role in regulating EC cell invasion through Epithelial-mesenchymal transition (EMT (show ITK Antibodies)) regulation.
S100A4 could promote the invasion ability of breast cancer cells via EMT (show ITK Antibodies), more importantly, it could participate in EMT (show ITK Antibodies) via regulating MMP2 (show MMP2 Antibodies) in breast cancer.
our results demonstrate not only that high expression of S100A4 contributes to an aggressive phenotype of EC, but also that its elevated expression is closely related to the MELF (show EPM2A Antibodies) histopathological pattern.
S100A4, A8, and A9 proteins represent promising marker genes to evaluate the risk potential of suspicious oral lesions in molecular pathology.
Increased S100A4 expression is associated with thyroid papillary carcinoma.
Comparative analysis of various tumor lines showed no clear correlation between the expression level of Mts1/S100A4 and the content of Oct-1 (show POU2F1 Antibodies). However, at stable transfection of tumor cells with Oct (show Plxna2 Antibodies)-1A, Oct (show Plxna2 Antibodies)-1L, and Oct (show Plxna2 Antibodies)-1X isoforms we detected an elevated level of Oct-1 (show POU2F1 Antibodies), which stimulated Mts1/S100A4 secretion.
We studied the expression of S100A4 and the total PHF10 (show PHF10 Antibodies) protein in some human cancer cell lines. We have found that, in the cell lines studied, the PHF10 (show PHF10 Antibodies) expression is correlated with the S100A4 expression.
These results support the hypothesis that S100A4 contributes significantly to growth and metastasis, and that down-regulation of S100A4 expression decreases the metastatic potential of ATC (show SRPK1 Antibodies) cells.
Interaction of extracellular S100A4 with RAGE (show AGER Antibodies) prompts prometastatic activation of melanoma cells.
Our results indicated that RNV was ameliorated by Ad-S100A4-RNAi transfer in a mouse model of OIR through mediation of the anti-apoptotic effect of Bcl-2 (show BCL2 Antibodies) by reducing the expression of CREB (show CREB1 Antibodies).
The thymic CD45 (show PTPRC Antibodies)-FSP1+ cells are a subpopulation of fibroblasts, which is crucial for the maintenance and regeneration of thymic epithelial cells.
Enhanced S100A4 expression was observed in remodeled intrapulmonary arteries of mice with smoke-induced emphysema.
Downregulation of AKT3 (show AKT3 Antibodies) increases migration and metastasis in triple negative breast cancer cells by upregulating S100A4.
S100A4 promotes liver fibrosis by activating HSCs, which may represent a potential target for anti-fibrotic therapies.
The S100A4 blocking antibody (6B12) reduces tumor growth and metastasis in a model of spontaneous breast cancer.
Functional studies of human TH2 cells as well as mouse models of allergy showed that deletion of one of the genes, S100A4, resulted in decreased signs of allergy.
S100A4 in endothelial cells is involved in tube formation, and suggest its potential as a molecular target for inhibiting tumor angiogenesis
S100A4 is overexpressed in an experimental head and neck squamous cell carcinoma, and its inhibition reduces tumor burden.
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 motility, invasion, and tubulin polymerization. Chromosomal rearrangements and altered expression of this gene have been implicated in tumor metastasis. Multiple alternatively spliced variants, encoding the same protein, have been identified.
S100 calcium binding protein A4
, S100 calcium-binding protein A4
, S100 calcium-binding protein A4 (calcium protein, calvasculin, metastasin, murine placental homolog)
, fibroblast-specific protein-1
, leukemia multidrug resistance associated protein
, malignant transformation suppression 1
, placental calcium-binding protein
, protein Mts1
, protein S100-A4
, S100 calcium binding protein A4 (calcium protein, calvasculin, metastasin, murine placental homolog)
, S100 calcium-binding protein A4 (calcium protein,calvasculin, metastasin, murine placental homolog)
, placental calcium-binding protein homolog
, metastatic cell protein
, protein 18A2
, Protein 9 Ka homologous to calcium-binding protein
, nerve growth factor-induced protein 42A