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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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.
If you have chosen panel analytes and then choose a premix or single plex kit, you will lose that customization.
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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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504395
Sigma-Aldrich(RS)-PPG - CAS 120667-15-4 - Calbiochem
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Description
Overview
A potent and subtype-selective agonist for group III metabotropic glutamate receptors. 25-fold higher selectivity for mGlu8 (EC50 =0.21 µM ) than for other group III mGlu receptors (EC50 = 5.2, 4.7, and 185 µM for mGlu4,6,7, respectively). Widely used as anticonvulsant, antidepressant, anxiolytic, and neuroprotective agent in research.
Catalogue Number
504395
Brand Family
Calbiochem®
Synonyms
(RS)-4-Phosphonophenylglycine
References
References
Gasparini, F., et al. 1999. J. Pharmacol. Exp. Ther.289, 1678. Palucha, A., et al. 2004. Neuropharmacology.46, 151. Bigge, C., et al. 1989. J. Med. Chem.32, 1580. Schoepp, D., et al. 1999. Neuropharmacology.38, 1431.
Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Toxicity
Standard Handling
Storage
+2°C to +8°C
Protect from Light
Protect from light
Do not freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C. Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Identification Number
Catalog Number
GTIN
5.04395.0001
4055977264081
Documentation
References
Reference overview
Gasparini, F., et al. 1999. J. Pharmacol. Exp. Ther.289, 1678. Palucha, A., et al. 2004. Neuropharmacology.46, 151. Bigge, C., et al. 1989. J. Med. Chem.32, 1580. Schoepp, D., et al. 1999. Neuropharmacology.38, 1431.
Data Sheet
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
28-June-2013 JSW
Synonyms
(RS)-4-Phosphonophenylglycine
Description
A potent and subtype-selective agonist for group III metabotropic glutamate receptors. 25-fold higher selectivity for mGlu8 (EC50 =0.21 µM ) than for other group III mGlu receptors (EC50 = 5.2, 4.7, and 185 µM for mGlu4,6,7, respectively). Widely used as anticonvulsant, antidepressant, anxiolytic, and neuroprotective agent in research.
Form
White powder
CAS number
120667-15-4
Chemical formula
C₈H₁₀NO₅P
Structure formula
Purity
≥97% by NMR
Solubility
DMSO (2 mg/ml)
Storage
Protect from light
+2°C to +8°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C. Stock solutions are stable for up to 3 months at -20°C.
Toxicity
Standard Handling
References
Gasparini, F., et al. 1999. J. Pharmacol. Exp. Ther.289, 1678. Palucha, A., et al. 2004. Neuropharmacology.46, 151. Bigge, C., et al. 1989. J. Med. Chem.32, 1580. Schoepp, D., et al. 1999. Neuropharmacology.38, 1431.