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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Although MALDI is more tolerant to contamination than other ionization methods, it is important to use reagents (e.g., matrix) and solvents of the highest purity so as to avoid making the analysis of the mass spectra more challenging than it already is.
Ions Ionic contamination, like Na+ and K+, will form adducts with the analytes and make data interpretation/analysis more challenging. Also, high salt concentration could affect crystallization of the matrix and analyte, leading to poor quality spectra.
Organics Some organics (detergents, polymers) could suppress the ionization of the analyte molecules. Detergents also disrupt the co-crystallization of matrix and analyte.
Bacteria Water for MALDI applications should be bacteria-free because they are sources of macromolecules (proteins, nucleic acids, carbohydrates) that could be detected by the mass spectrometer, complicating data analysis. They are also sources of ions and organics.
Experimental results
Figure 1 shows mass spectra of (A) cytochrome C, and (B) tryptic digest of bovine transferrin using a Bruker Autoflex MALDI-ToF instrument. Figure 2 was obtained in the reflectron mode. Ultrapure water from a Milli-Q® system was used to prepare the matrix.
Figure 1: MALDI-ToF spectra of (A) cytochrome C, and (B) tryptic digest of bovine transferrin using a Bruker Autoflex MALDI-ToF instrument.
Figure 2: Obtained in the reflectron mode.
Thus, even though MALDI ToF is known to be more tolerant than to ionic contamination compared to electrospray ionization, it is still important to use ultrapure water to obtain clean spectra.