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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Description
Overview
Useful as a differentiation marker of tumor cell growth. Protein kinase C inhibitor. Readily converted to GM1 by bacterial and mammalian neuraminidases without detergent or bile salts. Note: the moleculare weight is based on on stearoyl-18:0.
Catalogue Number
345736
Brand Family
Calbiochem®
Synonyms
Cer-Glc-Gal(NeuAc)-GalNAc-Gal-NeuAc ·2NH₄
References
References
Longee, D.C., et al. 1991. Acta Neuropathologica82, 45. Livingston, P.O., et al. 1987. Proc Natl. Acad. Sci. USA84, 2911. Kundu, S.K., and Scott, D.D. 1982. J. Chromato.232, 19. Wakomari, S. 1981. Annu. Rev. Biochem.50, 733.
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
05-September-2007 JSW
Synonyms
Cer-Glc-Gal(NeuAc)-GalNAc-Gal-NeuAc ·2NH₄
Description
Disialoganglioside prepared from bovine gray matter. Useful as a differentiation marker of tumor cell growth. Protein kinase C inhibitor. Readily converted to GM1 by bacterial and mammalian sialidases without detergent or bile salts. One mole yields 2 moles of sialic acid by thiobarbituric acid assay. The molecular weight is based on stearoyl-18:0.
Note: This product is not to be used for animal treatment, in vivo research, or in any other contact procedure with livestock.
Form
Lyophilized
Chemical formula
C₈₄H₁₄₆N₄O₃₉ · 2NH₄
Structure formula
Purity
≥98% by TLC
Solubility
Chloroform:Methanol (2:1) or DMSO. For use in aqueous systems, dissolve in a small amount of DMSO and then sonicate in buffer or medium, or dissolve the dried sample directly in aqueous buffers by sonication. Solutions may be filter sterilized.
Storage
-20°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, store in the refrigerator (4°C). Stock solutions are stable for up to 6 months at 4°C.
Toxicity
Irritant
References
Longee, D.C., et al. 1991. Acta Neuropathologica82, 45. Livingston, P.O., et al. 1987. Proc Natl. Acad. Sci. USA84, 2911. Kundu, S.K., and Scott, D.D. 1982. J. Chromato.232, 19. Wakomari, S. 1981. Annu. Rev. Biochem.50, 733.
