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.
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Filter material must be compatible with the chemical nature of the liquid being filtered under the conditions that the filtration will be performed. This will minimize the risk of structural failure during filtration.
Although chemical compatibility usually deals with the liquid phase of the sample, dissolved solutes may interact with the membrane in an undesirable manner. The solute of interest should not be adsorbed onto the surface of the filter. Most polymers used to make filters are highly adsorptive for biomolecules and will bind them out of the sample stream until the polymer surface is saturated. If a low binding surface is required, this property should be specified during the selection process.
In venting applications, hydrophobicity of a filter is used to allow release of air bubbles from a liquid stream. The sample stream should not contain detergents or solvents that will wet out the surface of the filter.
Membranes used in the filtration of organic solvents must be resistant to those solvents. If the membrane dissolves in the filtration process, that membrane will be totally useless in filtering those solvents.
When selecting a filter, determine if constituents in the sample will chemically attack the filter. If the filter undergoes chemical degradation, it may release foulants into the sample stream.
Some solvents may be incapable of dissolving the filter, but could be absorbed into the polymer matrix causing it to swell over time and altering the effective pore size of the filter and changing its performance.
Aqueous liquids
The same is true of an aqueous stream. Care must be taken that the filter not be damaged by the aqueous stream. Most membrane polymers are resistant to standard water. Issues arise when the pH of the water is incorrect, or when additives chemically attack the polymer.
Determine if the filter is sensitive to extremes of pH and compatible with specific acids and bases. Chemical attack at extremes of pH may take time to appear and could be problematic well before filtration is completed.