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.
3 Relatively unreactive organic reagents should be collected in container A. If halogenated, they should be collected in container B. For solid residues use container C.
Safety Information
Product Usage Statements
Storage and Shipping Information
Storage
Store at +15°C to +25°C.
Packaging Information
Transport Information
Supplemental Information
Specifications
Appearance
white to almost white, crystalline powder
Assay (alkalimetric, calculated on dried substance)
≥ 99.0 %
Identity (IR-spectrum)
conforms
pH-value (0.5 mol/l, water)
3.5 - 5.0
Melting point
147 - 153 °C
UV-Absorption (230 nm; 10 %; 1 cm; water)
≤ 0.1
UV-Absorption (260 nm; 10 %, 1 cm; water)
≤ 0.06
UV-Absorption (280 nm; 10 %; 1 cm; water)
≤ 0.06
UV-Absorption (300 nm; 10 %; 1 cm; water)
≤ 0.02
UV-Absorption (400 nm; 10 %; 1 cm; water)
≤ 0.01
Residual solvents (ICHQ3C) of class 2 (Methanol)
≤ 3000 ppm
Residual solvents (ICHQ3C) of class 2 (Nitromethane)
≤ 50 ppm
Residual solvents (ICHQ3C) of class 3 (Ethanol)
≤ 5000 ppm
Residual solvents (ICHQ3C) of class 3 (Ethylmethylketon)
≤ 5000 ppm
Other residual solvents (ICH Q3C)
excluded by manufacturing process
Sulfated ash
≤ 0.03
Loss on Drying (105°C)
≤ 0.5
Endotoxins
< 2.5
Total aerobic microbial count
≤ 10²
Total yeast and mould count
≤ 10²
Salmonella spp.
absent in 10 g
E.coli
absent in 1 g
Staphylococcus aureus
absent in 1 g
Pseudomonas aeruginosa
absent in 1 g
Candida albicans
absent in 1 g
Bile tolerante gram negative bacteria
absent in 1 g
DNases (Exo- and endonucleases)
not detected
Proteases
not detected
RNases
not detected
Elemental impurity specifications have been set considering ICH Q3D (Guideline for Elemental Impurities). Class 1-3 elements are not likely to be present above the ICH Q3D option 1 limit, unless specified and indicated (*).
Total yeast and mould count
≤ 10²
Salmonella spp.
absent in 10 g
E.coli
absent in 1 g
Staphylococcus aureus
absent in 1 g
Pseudomonas aeruginosa
absent in 1 g
Candida albicans
absent in 1 g
Bile tolerante gram negative bacteria
absent in 1 g
DNases (Exo- and endonucleases)
not detected
Proteases
not detected
RNases
not detected
Elemental impurity specifications have been set considering ICH Q3D (Guideline for Elemental Impurities). Class 1-3 elements are not likely to be present above the ICH Q3D option 1 limit, unless specified and indicated (*).
