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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You can now customize another kit, choose a premixed kit, check out or close the ordering tool.
The SNAP i.d.® 2.0 protein detection system replaces the traditional immunodetection phase of western blotting. Use the SNAP i.d.® 2.0 to increase antibody-antigen binding, enhance washes and increase antibody recollection. With our vacuum transport feature, researchers can do fluorescent, chemiluminescent or chromogenic detection in a fraction of the time.
See what our customers are saying about the SNAP i.d.® Protein Detection Systems.
Steve Thibault, Amgen Principal scientist describes how the SNAP i.d.® 2.0 system has improved his protein detection protocol over traditional Western blotting methods.
"SNAP id system for western blotting is working great. This is very quick and productive system to identify the proteins. The only thing we need to optimize conditions for each antibody. This is little bit expensive" - T. Madanayake, New Mexico State University, USA
"The SNAP i.d.® system from Millipore is a great innovation. It is fast and easy, a perfect tool in a teaching lab. It has significantly reduced the amount of time detecting Western blots." - K. Duong-Polk, University of California, San Diego, USA
"Quick and easy to do Western Blots with SNAP i.d.®, however, sometimes blots are really faint when developed, some primary antibodies need more time then a few min to bind. Need to test those antibodies and maybe leave them a bit longer to bind. Otherwise, really makes things faster when doing W.B." - G. Cseke, Heptares Therapeutics, UK Biocompare Review
Got something interesting to share about the SNAP i.d.® protein detection systems? We’d love to hear more!