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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Add Additional Reagents (Buffer and Detection Kit is required for use with MAPmates)
Buffer Detection Kit for Magnetic Beads
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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Sample preparation of macromolecule solutions, such as proteins, enzymes, antibodies, and viruses, often yield large volumes of diluted macrosolutes in buffers that are incompatible with downstream processes or detection.
Centrifugal ultrafiltration devices (such as the Amicon® Ultra Filters) are regularly used to concentrate and buffer-exchange these types of macrosolutes; however, volumes larger than 50 mL present significant challenges, requiring samples to be loaded in multiple stages or aliquoted over several devices.
The Amicon® Stirred Cell family of pressure-driven filtration devices provide an ideal solution for concentrating and buffer-exchanging large volumes of macrosolutes. These devices are available in multiple sizes to offer a wide range of processing volumes. To process even larger volumes, an external reservoir can be attached to any Amicon® Stirred Cell.
The new generation of Amicon® Stirred Cells provides ergonomic benefits, integrated safety features, a more secure stir bar, superior integrity, and ease of use while also providing a broader selection of membrane discs.
Simultaneous Sample Concentration and Buffer Exchange by Ultrafiltration Plus Diafiltration
Ultrafiltration is a proven method for sample concentration. When combined with diafiltration, the analyte of interest is provided at a concentration and in a buffer that is compatible with additional purification and analysis steps. During ultrafiltration, the desired macrosolute concentration is achieved because the concentration of non-permeating species is increased while the fluid volume is reduced. Furthermore, the concentration of membrane-permeating species such as salts and microsolutes remains unchanged.
How to Choose the Correct Ultrafiltration Membrane (NMWCO) for the Sample
When using ultrafiltration for sample concentration, particular attention has to be paid in choosing the correct membrane molecular weight cut-off, as well as membrane material. Ultrafiltration membranes are typically made from regenerated cellulose or polyethersulfone (PES). The material of choice will greatly depend on sample compatibility. The choice of membrane nominal molecular weight cut-off (NMWCO) will depend on the molecular weight (MW) of the macrosolute that is to be retained. Membrane choice will have a significant impact on performance. As a rule, the NMWCO should be 2-3 times smaller than the molecular weight of the solute to be retained when using regenerated cellulose and 4-5 times smaller for Biomax® PES membranes.
Solute retention may be further influenced by:
You may need to optimize the above parameters to assure desired yield. The most frequently used ultrafiltration membranes have a NMWCO range of 3 kDa to 100 kDa, although smaller and larger pore sizes are available.
Diafiltration Compared to Dialysis
Diafiltration is a technique that uses ultrafiltration for buffer exchange. Diafiltration can rapidly and efficiently eliminate salts and/or microsolutes from macromolecular mixtures. This process is typically called “washing out.”
The term “washing in” is used when diafiltration is employed to replace one salt species or microsolute with another, as is done during buffer exchange.
Traditional dialysis is an alternative buffer exchange technique; however, it has several drawbacks:
It relies on slow diffusion and difficult-to-handle dialysis tubing or cassettes.
In many cases, during the course of dialysis, the volume in the dialysis tubing increases as a consequence of osmosis, further diluting the sample and requiring a sample concentration step.
Dialysis can require large buffer volumes and multiple buffer changes.
In contrast, diafiltration uses ultrafiltration membranes, either in centrifugal or pressure-driven devices such as the Amicon® Stirred Cell, for efficient buffer exchange.
Advantages of diafiltration using stirred cell ultrafiltration:
Unlike dialysis tubing, ultrafiltration membranes can be used for both sample concentration as well as buffer exchange
Minimizes sample transfers and reduces sample loss.
Diafiltration often requires significantly less buffer volume than traditional dialysis.
Transport convective with solvents, independent of microsolute composition
Transport diffusion-controlled, dependent on type of microsolute
Smaller volume of exchange buffer required
High volume of exchange buffer volume required, efficient mixing and frequent buffer changes required to drive efficient transport
Rapid exchange rate. Fractional removal of solvent microsolute is independent of sample composition
Exchange rate is slow and efficiency is reduced with decrease microsolute concentration
Ultrafiltration rate reduced with decreased temperature
Reduced microsolute transport with decreased temperature
At high macrosolute content, ultrafiltration rate and microsolute transport are reduced
Microsolute transport unaffected by content of retained Macrosolutes
Scalable; compatible with samples ranging from few microliters to many liters
Not easily scalable to large volume, best used for microliter-to-liter volume samples.
Continuous vs. Discontinuous Diafiltration
Diafiltration can be performed in either continuous or discontinuous mode. Discontinuous diafiltration refers to a practice where the sample is first concentrated, then diluted with exchange buffer to the initial starting volume, followed by another concentration step. This process is repeated until the desired microsolute has been exchanged.
On the other hand, continuous diafiltration maintains a constant volume throughout the buffer exchange process, by introducing exchange buffer at the same rate as filtrate is being removed. By maintaining a fixed volume, the retained solute concentration remains constant, providing a gentler method of buffer exchange.
In general, continuous diafiltration is more efficient than discontinuous diafiltration. In discontinuous diafiltration, the permeate flux decreases as the sample concentration increases, which can contribute to membrane fouling and cause increased retention of microsolutes that would otherwise pass through the membrane.
Calculating Buffer Exchange Volume for Continuous Diafiltration
The buffer requirement during diafiltration is typically expressed as “diafiltration volume” (DV). The DV is equal to the volume of the permeate removed during diafiltration divided by the volume of the remaining retentate (Equation 1).
Microsolutes that are partially retained by the membrane will require additional DV. As a general rule of thumb, using DV=three times the sample volume will wash out 95%, and using DV=five times the sample volume will remove 99% of a non-retained microsolute.
Equation 2 can be used for theoretical calculations of diafiltration volume requirements. However, these are guidelines and actual diafiltration volume requirements need to be empirically determined.
Buffer Requirements for Continuous Diafiltration
Calculating Buffer Exchange Volume for Discontinuous Diafiltration
In discontinuous diafiltration, salt and microsolute removal depend on the degree of concentration during the repeated concentration/dilution steps. The microsolute level decreases according to Equation 3 during each step.
Example: A 100 mL of a 1 mg/mL bovine serum albumin (BSA) protein sample containing 1 M salt is concentrated down to 50 mL, concentrating the protein to 2 mg/mL while the salt concentration is constant at 1 M. Then, the sample is diluted back to 100 mL, reducing BSA concentration to 1 mg/mL and the salt concentration down to 0.5 M. Each diafiltration step reduces the salt concentration by 50%.
These two steps are repeated until the salt has been reduced to the desired concentration.
The salt concentration after each step can be calculated using Equations 3 and 4:
The above should be viewed as a guideline, as sample types and composition vary greatly and overconcentration could have detrimental consequences.
While continuous diafiltration is traditionally used with large volume tangential flow filtration (TFF) systems, you can use this gentle form of buffer exchange with the Amicon® Stirred Cell.
The same reservoir used to extend the processing volume during sample concentration can now be used for the diafiltration buffer. Once pressure has been applied and equalized throughout the setup, exchange buffer will enter the stirred cell at the same rate at which the permeate is being removed.