ANTI-FLAG. HS, M2 COATED 96-WELL PLATES&

Description_x000D_ General description_x000D_ The Anti-FLAG® HS, M2 Coated Plates are designed to ensure a higher binding capacity than other plates. This is due to the orientation of the Anti-FLAG® M2 mouse monoclonal IgG1 antibody on the plates. The antibody is covalently linked to the surface of a microtiter plate via the Fc portion of the antibody._x000D_ Application_x000D_ ANTI-FLAG® High Sensitivity, M2 coated 96-well plates is used for Enzyme-linked immunosorbent assays. A convenient, ready to use, platform for the capture and detection of FLAG® fusion proteins. The ANTI-FLAG® M2 antibody is covalently attached to the surface through the Fc portion and can detect 1 ng FLAG fusion protein/well with a capacity of up to 300ng/well. Suitable for screening for expression, study of protein:protein interactions and ELISA assays. Manufactured under ISO 9002 in Sigma′s GMP facility, ANTI-FLAG®P2983 high sensitivity M2 coated multiwell plates utilize a flat bottom, polystyrene baseplate._x000D_ Browse additional application references in our FLAG® Literature portal._x000D_ Storage and Stability_x000D_ Once plates are opened, they should be stored with desiccant at 2- 8 °C and used within two weeks._x000D_ Legal Information_x000D_ ANTI-FLAG is a registered trademark of Sigma-Aldrich Co. LLC_x000D_ F-127 is a registered trademark of BASF SE_x000D_ FLAG is a registered trademark of Sigma-Aldrich Co. LLC_x000D_ Other Notes_x000D_ Components:_x000D_ The plate is supplied as a 96-well microtiter plate with clear sides and bottom._x000D_ Coating:_x000D_ ANTI-FLAG® M2 mouse monoclonal antibody, IgG1, is coated at a reaction volume of 200 ml/well._x000D_ Blocking:_x000D_ The wells are pre-blocked for convenience at 275 to 300 ml/well with a complex solution containing bovine serum albumin._x000D_ Specificity:_x000D_ The plates are specific for the FLAG epitope regardless of its placement in the fusion protein: amino-terminal, Met-amino terminal, carboxy terminal or internal. Binding of the epitope is not Ca2+ dependent._x000D_ Sensitivity:_x000D_ Detection of 1 ng/well of a control fusion protein was observed in an ELISA format with p-Nitrophenyl Phosphate (pNPP) as a substrate._x000D_ Capacity:_x000D_ Capture of 100 to 300 ng/well of a FLAG fusion protein has been demonstrated.