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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69237
Sigma-AldrichHuman Genomic DNA
High molecular weight, high purity DNA for any application
More>>High molecular weight, high purity DNA for any application Less<<
Human Genomic DNA MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
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Description
Overview
Genomic DNAs are highly purified preparations of high molecular weight genomic DNA from a variety of organisms. The isolation protocol minimizes shearing and removes contaminants that inhibit enzymatic procedures. Novagen genomic DNA is qualified for genomic analysis (including PCR) and library construction. At least 90% of the DNA is greater than 100 kbp in size, as analyzed by CHEF gel electrophoresis (> 50 kbp for S. cerevisiae). No inhibition of restriction enzyme activity is observed, and the DNA is free of contaminating RNA and protein.
The DNA is supplied in 10 mM Tris-HCl, pH 8.0, 1 mM EDTA (TE). Pipet with a wide-bore
pipet tip to minimize shearing.
Hilke Zander, et al. (2007) Biochemical characterization of the recombinant human Nogo-A ectodomain. Federation of American Societies for Experimental Biology Journal274, 2603.
