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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Denaturating HPLC is a reverse-phase ion pairing HPLC method used to study single nucleotide polymorphism in DNA molecules. It is an alternative to gel electrophoresis methods used to detect mutations. This method commonly resolves heteroduplexes and homoduplexes of DNA fragments ranging from 200 bp to 1000 bp. Larger fragments can be resolved in some cases. The resolution is based on differences in size and on differences in helical composition induced by temperature-modulated denaturation at 50 °C to 70 °C. The use of DHPLC for heteroduplex mutant analysis provides advantages, such as specificity, sensitivity and high throughput that can increase productivity in the screening of genetic loci.
The thermally less stable heteroduplexes denature more extensively and, therefore, are retained a shorter time on the stationary phase. The eluent contains the cationic TEAA ion (0.1 M), which interacts with the negatively charged phosphate groups on DNA molecules and also with the hydrophobic surface of the particles in the columns. The TEAA ion can be described as a bridging molecule between DNA fragments and the column. As the mobile phase is made progressively more organic, the DNA fragments are eluted in order of size.
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