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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Many biological responses are initiated through direct cell-cell interactions. Such interactions may result in the recruitment of signaling molecules to the interacting point of contact (such as at the immune synapse), or in transfer of materials between cells, or cellular fusion. These systems are naturally suited for microscopic analysis, and the high speed image acquisition and quantitative image analysis capabilities of Amnis® imaging flow cytometers bring major advances to the study of cell-cell interactions. Single cells, conjugates, and fusion events are easily distinguishable in statistically significant sample sizes, and accumulation of protein at the synapse or transfer of material between two cells readily identified and quantified.
Watch to learn how multispectral imaging in flow can be used to answer specific cell interaction research questions. Dr. Sherree Friend explains how Amnis® applications use high-throughput imaging to characterize cell-cell interaction events. Using antigen presenting cells activated with enterotoxin B and incubated with T cells, microscopy in flow can be used to enhance analysis of the immune synapse.
Ovalbumin Specific T Cells Incubated with Antigen Presenting Cells +/- Ovalbumin Peptide
Ovalbumin-specific accumulation of ADAP at the immune synapse is measured. Quantitation of conjugate formation and representative cell images show that without specific peptide, ADAP (green) is distributed around the T cell. In the presence of specific peptide, ADAP moves to the synapse between the APC and T cell.
Membrane Transfer Between Cells
Transfer of PKH26 labeled cell membrane (red) from antigen presenting cells (APC) to T cells identified by CD3 (green). Cell images show T cell:APC conjugates (gate R8) and single T cells with APC membrane material (gate R3).