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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SNAP i.d.® ProteinDetection 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.
RNA-binding protein immunoprecipitation (RIP) is the RNA analog of the ChIP application (chromatin immunoprecipitation). It can be used to identify specific RNA molecules (of many types) associated with specific nuclear or cytoplasmic binding proteins.
Protein oxidation is frequently associated with excess oxidative stress in the cell. Our protein oxidation detection kits in WB (OxyBLOT™), Elisa (OxyELISA™), ICC (OxyICC), and IHC (OxyIHC) formats detect carbonyl groups introduced on proteins.
Protein phosphorylation systems are composed of at least three components: (a) phosphoproteins (b) kinases and (c) phosphatases, that dephosphorylate the phosphoproteins, thereby restoring the system to its basal stage.
The SNAP id 2.0 proteindetection system uses a vacuum to drive reagents through the membrane, enabling increased antibody-antigen binding, enhanced washes, and antibody recollection.
Our bacteria protein extraction reagent is a detergent mix capable of cell wall perforation without denaturing soluble protein, with an incubation time of 10 minutes.
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.
For mammalian protein extraction, we provide a proprietary formulation of detergents optimized for fast extraction of soluble proteins, anda nuclear protein extraction kit.
Learn about our proteindetection platforms, including our Direct Detect spectrometer, optimized Western blotting reagents and instruments and multiplex instruments for Luminex xMAP bead-based detection