Our broad portfolio consists of multiplex panels that allow you to choose, within the panel, analytes that best meet your needs. On a separate tab you can choose the premixed cytokine format or a single plex kit.
Cell Signaling Kits & MAPmates™
Choose fixed kits that allow you to explore entire pathways or processes. Or design your own kits by choosing single plex MAPmates™, following the provided guidelines.
The following MAPmates™ should not be plexed together:
-MAPmates™ that require a different assay buffer
-Phospho-specific and total MAPmate™ pairs, e.g. total GSK3β and GSK3β (Ser 9)
-PanTyr and site-specific MAPmates™, e.g. Phospho-EGF Receptor and phospho-STAT1 (Tyr701)
-More than 1 phospho-MAPmate™ for a single target (Akt, STAT3)
-GAPDH and β-Tubulin cannot be plexed with kits or MAPmates™ containing panTyr
.
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Select A Species, Panel Type, Kit or Sample Type
To begin designing your MILLIPLEX® MAP kit select a species, a panel type or kit of interest.
Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
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96-Well Plate
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Add Additional Reagents (Buffer and Detection Kit is required for use with MAPmates)
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48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
Space Saver Option Customers purchasing multiple kits may choose to save storage space by eliminating the kit packaging and receiving their multiplex assay components in plastic bags for more compact storage.
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Highly polar or ionizable chemical groups increase the colloidal stability of the microspheres suspension and allow covalent binding of polyclonal or monoclonal antibodies, proteins and haptens. In comparison to physical adsorption, covalent binding of antigens or antibodies to polymer microspheres improves the test performance, and the reagents produced are more stable over time.
Moreover, microspheres with specific functional groups on their surface can bind proteins covalently in the appropriate orientation, directly or by additional activation, giving more sensitive and specific immunoreagents. Some of the surface groups able to covalently bound directly amino acid protein residues are chloromethyl; or after preactivation with carboxy, amino or hydroxy groups.
Due to their more hydrophilic surface, our functionalized polymer microspheres have very low non-specific binding, and a better signal-to-noise ratio.
Carboxyl–modified white microspheres (–COOH)
Highly polar or ionisable chemical groups increase latex stability and also facilitate covalent coupling of proteins to the microsphere surface.
The groups –COOH are produced by copolymerisation of the corresponding functional monomers. For carboxylated latexes, eliminating surfactant and lowering pH decrease latex stability and may trigger partial flocculation. In this case, we recommend diluting the latex further and slowing the stirring. If the result is still unsatisfactory, a non-ionic emulsifier may be added. (0.1 to 0.5 g/L of TWEEN 20).
Amino–modified white microspheres (–NH2)
Highly polar or ionisable chemical groups increase latex stability and also facilitate covalent coupling of proteins to the microsphere surface.
The groups –NH2 are produced by copolymerisation of the corresponding functional monomers.
Chloromethyl–modified white microspheres (–CH2Cl)
Highly polar or ionisable chemical groups increase latex stability and also facilitate covalent coupling of proteins to the microsphere surface.
The groups –CH2Cl are produced by copolymerisation of the corresponding functional monomers.
Hydroxy-modified White Estapor® Microspheres (–OH)
Highly polar or ionisable chemical groups increase latex stability and also facilitate covalent coupling of proteins to the microsphere surface.
The groups –OH are produced by copolymerisation of the corresponding functional monomers.