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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The SNAP id 2.0 protein detection system uses a vacuum to drive reagents through the membrane, enabling increased antibody-antigen binding, enhanced washes, and antibody recollection.
Prior to probing a membrane using precious antibodies, it is helpful to visualize the transferred proteins on the blot to ensure complete transfer and even loading. This page describes possible causes and potential remedies for challenges encountered during protein visualization.
The possible causes and potential remedies for challenges encountered dot/slot blotting, which uses vacuum filtration to transfer protein onto a microporous membrane.
The possible causes and potential remedies for challenges encountered during preparation of samples for SDS-PAGE (sodium dodecyl sulfate polyacrylamide gel electrophoresis) and optimizing electrophoresis conditions.
Learn how SNAP id 2.0 protein detection system works, which applications it is compatible with, and how it optimizes westernblotting conditions for reduced workflow.
This page describes common challenges encountered when lysing cells and extracting proteins prior to Westernblotting. Total protein concentration must be determined for these cell lysates. Variables affecting each of these steps are outlined below, as each could affect the sensitivity and reproducibility of the Westernblot.
The possible causes and potential remedies for challenges encountered as a result of blocking, washing, antibody incubation, and detection/exposure of Westernblots.
An online troubleshooting guide describing the most common symptoms of Westernblots that exhibit poor signal-to-noise, poor reproducibility, or other obstacles to interpretation. Choose a topic to view possible causes and potential remedies.
Merck's novel SNAP i.d.® 2.0 Protein Detection System can streamline the immunodetection reagent application phases of both Westernblotting and IHC using a controlled vacuum force that removes solutions evenly - in seconds.
SNAP i.d.® Protein Detection System for Immunohistochemistry (IHC) is the latest capability of the SNAP i.d.® 2.0 System. It allows you to process up to 24 slides at a time with reduced handling time and variability. The system is compatible with standard IHC slides and protocols and works with diverse tissue preparations including formalin-fixed and fresh frozen samples. Watch this video for an introduction to the innovative, vacuum driven system for IHC.