IgA Secretory Component / ECM1 Antibody - Without BSA and Azide
Mouse Monoclonal Antibody [Clone SC05 ]
|Application ||IHC-P, IF, FC|
|Other Accession||1893, 81071|
|Isotype||Mouse / IgG1, kappa|
|Other Names||Extracellular matrix protein 1, Secretory component p85, ECM1|
|Format||200ug/ml of Ab purified from Bioreactor Concentrate by Protein A/G. Prepared in 10mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml.|
|Storage||Store at 2 to 8°C.Antibody is stable for 24 months.|
|Precautions||IgA Secretory Component / ECM1 Antibody - Without BSA and Azide is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Involved in endochondral bone formation as negative regulator of bone mineralization. Stimulates the proliferation of endothelial cells and promotes angiogenesis. Inhibits MMP9 proteolytic activity.|
|Cellular Location||Secreted, extracellular space, extracellular matrix|
|Tissue Location||Expressed in breast cancer tissues. Little or no expression observed in normal breast tissues. Expressed in skin; wide expression is observed throughout the dermis with minimal expression in the epidermis.|
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Provided below are standard protocols that you may find useful for product applications.
This MAb reacts with a reduction-resistant epitope present in both free and SIgA bound Secretory Component. It does not react with the cell lines lacking secretory component. The antibody is useful for studying the distribution and level of both free and bound secretory component. Secretory component is differentially expressed in epithelium, and the antibody is a popular marker for identifying subpopulations of epithelial cells and epithelial differentiation. The Secretory component antibody is a useful research tool for studying mucosal immunity, inflammation, remodeling, differentiation and tumorigenesis, all processes associated with differential secretory component expression.
Bartek J et. al. Histochemistry 91:235-244 (1989). | Int. J. Cancer, 42, 638-641 (1988). | Histochem J., 22, (1990)
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