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
.
Catalogue Number
Ordering Description
Qty/Pack
List
This item has been added to favorites.
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.
Catalogue Number
Ordering Description
Qty/Pack
List
This item has been added to favorites.
Species
Panel Type
Selected Kit
Qty
Catalogue Number
Ordering Description
Qty/Pack
List Price
96-Well Plate
Qty
Catalogue Number
Ordering Description
Qty/Pack
List Price
Add Additional Reagents (Buffer and Detection Kit is required for use with MAPmates)
Qty
Catalogue Number
Ordering Description
Qty/Pack
List Price
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.
This item has been added to favorites.
The Product Has Been Added To Your Cart
You can now customize another kit, choose a premixed kit, check out or close the ordering tool.
Attention: We have moved. Merck Millipore products are no longer available for purchase on MerckMillipore.com.Learn More
Nuclease-free water is used in assays and experiments involving nucleic acids. Nucleases include DNases, specific for DNA degradation, and RNases, specific for RNA degradation. These enzymes can degrade the nucleic acids from an extremity of the strand or from the middle of the strand, and are called respectively exonucleases and endonucleases. In situ, RNases degrade foreign nucleic acids, regulate gene expression by degrading mRNA, have some antitumor activity and mature various RNA.
Several classes of these enzymes exist in bacteria, with various selectivity and activity. In water, nucleases originate from bacteria, and the molecular weight of the bacterial RNases may vary significantly. For instance RNAse I has a molecular weight of 27 000 Da, while RNase III has two 26 500 Da subunits.
These enzymes are extremely active and a small amount of those nucleases will generate the degradation of the nucleic acids present in the samples. It is therefore particularly important to keep the sample, buffers, plasticware and glassware, benches, and all containers free of nucleases at all times. Water, as the major component of the buffers utilized for the assays should be nuclease-free.
Nuclease-free water has typically been prepared via DEPC (diethylpyrocarbonate) treatment of the buffers. Enzymes are inactivated during the process, as the nitrogen atoms from histidine residues of the RNase active site reacts with the DEPC. Because the nitrogen reacts with DEPC, buffers based on amine containing compounds, such as HEPES and Tris cannot undergo DEPC treatment. Following the inactivation step, the excess of DEPC is eliminated by a 1 h autoclaving step.
By-products of the chemical inactivation, as well as by-products generated during the autoclaving include ethanol and CO2, which reacts with water to generate carbonic acid and bicarbonate. Therefore, both DEPC-treatment by-products impair the water quality: ethanol contributes to the TOC, and bicarbonate increases the conductivity.
Figure 1: Degradation of DEPC yields to water contamination
Feel free to express your comments
Your opinion is important to us. Let us know if this information was useful, or if there was something missing that you'd like to see. Contact us.