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.
If you have chosen panel analytes and then choose a premix or single plex kit, you will lose that customization.
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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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You can now customize another kit, choose a premixed kit, check out or close the ordering tool.
Attention: We have moved. EMD Millipore products are no longer available for purchase on emdmillipore.com.Learn More
Immunostaining of human pancreas tissues using Anti-PER2, clone 7H4.1 (Cat. No. MABS462). Endocrine cells in islets of Langerhans of human pancreas were seen with positive nuclear and cytoplasmic staining.
Current chronobiology research suggests that a multitude of diverse organ systems and tissue types seem to vary their physiology in a cyclical, daily clock-like rhythm. Individual clock mechanisms may be tied to a ‘master clock’ that synchronizes the various rhythms with external cues like light and temperature. The neurobiology underlying this circadian rhythm is under intense study, and includes key hypothalamic players (SCN) and pineal gland, retinal and extraretinal receptor pathways. Recent discovery of encephalopsins, melanopsins, Per and CLOCK gene variants, and intrinsically photosensitive retinal ganglion cells (ipRGCs), suggests a complicated and phylogenetically diverse set of circadian control mechanisms.
