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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DNA sequencing mimics the basic process used to copy DNA in a cell during chromosomal replication, except that the procedure is done in a tube or microtiter plate using a minimal set of components. Most DNA sequencing techniques require that there be a "template", (i.e., a biological sample of the DNA whose sequence is to be determined); a "primer", (i.e., a short oligonucleotide that is complementary to a region of the template and capable of being extended); and a DNA polymerase enzyme that successively adds building blocks on to a primer, as directed by the template strand; and the four building blocks themselves. The technique also must embody a method by which the order of the building blocks added to the primer can be detected. Using the detection method of choice, the sequence of the DNA strand complementary to the template is, thereby, determined.
Most large-scale DNA sequencing facilities use fluorescent dyes to label and detect the four bases, and capillary electrophoresis to separate DNA molecules on the basis of size so that the base located at each position in the sequence can be identified. More specifically, for a small percentage of the molecules of each building block added to the sequencing reaction, the building block is chemically modified and labeled with a distinguishable dye such that when a modified building block is randomly added to the DNA strand being extended from the primer, the replication "terminates", with the result that the sequencing reaction contains a mixture of molecules of varying sizes. Because the end of each terminated molecule contains a dye-labeled base, the sequence of the strand complementary to the template can be determined.
The image above shows a set of sequencing lanes, where electrophoresis is used to separate molecules differing by one base. Laser detection is used to identify the bases at each position. The sequence is "read" from the bottom up, using a key where "A" is green, "C" is blue, "G" is yellow, and "T" is red. Using software provided by the manufacturers of sequencing machines, the signal/noise ratios of the dyes is determined for each position so that the proper base can be "called". The order of the bases is displayed in a "chromatogram" or "trace" file.
More Information
You may find more information related to DNA sequencing in the following web site: