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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The water contaminants that affect HPLC also impact UHPLC, but to a more significant extent in some cases.
Particles The effect of particles become more significant in UHPLC, with its smaller particle sizes, lower interstitial void volumes, decreased column diameters and higher flow rates. Columns filled with very small particles are more susceptible to premature plugging by particulates compared to their HPLC column counterparts with larger particles.
Organics Organics contamination of the ultrapure water may affect chromatographic separations different ways:
Organic molecules may accumulate on the surface of the chromatography column beads, slowing down the access of sample and solvent molecules to the binding sites located inside the pores of the beads. This causes mass transfer issues and results in a loss of resolution and ultimately in a shorter column life time.
Organic molecules in the water used as an eluent may compete with the sample molecules for binding to the active groups on and in the chromatography beads. The consequence is that less sample molecules are bound during the injection and binding phase and therefore less sample molecules are released during the elution process. As a result, the sensitivity of an analytical chromatography method can be reduced by the presence of organics in the water used for chromatographic separations.
Organics may accumulate at the head of the column and later on elute as contaminant/ghost peak(s). If the level of organic contamination is very high, the contaminant(s) may act like a new stationary phase, causing shift in retention time and peak tailing. Accumulation of organic material in the column may also lead to back pressure increase.
For all these reasons, it is critical to monitor accurately the level of organics in water used for HPLC applications and this can conveniently be performed by an on-line TOC monitor.
Colloids Colloids may adsorb irreversibly on the stationary phase, thereby losing its original separation efficiency of the column.
Bacteria Bacteria may plug column and frits and release organic by-products (see effects of organic contamination)
Ions Contamination Ion contamination will also affect chromatographic separations. A modification of the ionic strength of the solution may affect some separations, and if the ionic contaminant is UV-absorbing ions (e.g., nitrates, nitrites), it will come out as peak and make data analysis difficult. If using a mass spectrometer as detector, formation of adducts other than the protonated one (e.g., Na+, K+ adducts) could make data analysis more difficult.
Other Sources of Contamination
Storage of Ultrapure Water Storing ultrapure water will introduce leachables to the water. Plastic containers leach out organics and some ions. Glass containers do not leach out as much organics, but they can introduce ions into the water. Storing ultrapure water would also encourage the proliferation of bacteria.
Solvent Additives Additives like trifluoracetic acid (TFA) are often added to the solvent to enhance ionization in LC-MS. Salts to make buffers are also commonly used. Only the highest quality reagents should be chosen.