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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You can now customize another kit, choose a premixed kit, check out or close the ordering tool.
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Traditional peptide quantitation can be inaccurate.
Determining peptide concentration accurately and quickly has proven difficult for many researchers. Most commonly used methods for peptide quantitation rely on the weight of the lyophilized powder, absorbance of ultraviolet (UV) light or amino acid analysis. Establishing peptide concentration based on the weight of the lyophilized peptide is inaccurate in most cases, because the analyzed powder can contain a significant quantity (10-70%) of bound water, salts or counterions. Another peptide quantitation method relies on absorbance at 280 nm, and thus can only be used to estimate peptide concentration if tryptophan and tyrosine resides are present in the sequence. Therefore, peptides that do not contain amino acids that absorb light at 280 nm cannot be accurately quantified using this method.
Benefits of Using Direct Detect® Spectrometer for Peptide Quantitation
The Direct Detect® spectrometer provides a universal, fast and accurate peptide quantitation method that does not require sample manipulation. IR spectroscopy exploits the fact that molecules absorb specific frequencies characteristic of their structure. To form a peptide, amino acids are covalently linked via amide (peptide) bonds. In order to determine protein and peptide concentration, the Direct Detect® spectrometer uses the intensity of the Amide I band, which is assigned to C=O stretching vibration of the peptide bond (about 80%) with a minor contribution from C-N stretching vibration (about 20%).