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.
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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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504394
Sigma-AldrichAIDA - CAS 168560-79-0 - Calbiochem
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Description
Overview
A relatively potent and selective antagonist for group I mGlu receptor subtype 1 (pKB = 3.4 for mGlu1a). Complete absence of interacting with on group II or III mGluRs, or ionotropic glutamate receptors. Widely used in studying neural plasticity, learning and memory, and fear conditioning. Centrally active following systemic administration in vivo.
Catalogue Number
504394
Brand Family
Calbiochem®
Synonyms
(RS)-1-Aminoindan-1,5-dicarboxylic acid, UPF 523
References
References
Pellicciari, R., et al. 1995. J. Med. Chem.38, 3717. Moroni, F., et al. 1997. J. Pharmacol. Exp. Ther.281, 721. Nielsen, K., et al. 1997. Eur. J. Pharmacol.326, 105.
Christoffersen, G., et al. 1999, Neuropharmacology.38, 817.
Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Toxicity
Standard Handling
Storage
+15°C to +30°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 Item Number
Catalogue Number
GTIN
5.04394.0001
04055977264074
Documentation
References
Reference overview
Pellicciari, R., et al. 1995. J. Med. Chem.38, 3717. Moroni, F., et al. 1997. J. Pharmacol. Exp. Ther.281, 721. Nielsen, K., et al. 1997. Eur. J. Pharmacol.326, 105.
Christoffersen, G., et al. 1999, Neuropharmacology.38, 817.
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)-1-Aminoindan-1,5-dicarboxylic acid, UPF 523
Description
AA relatively potent and selective antagonist for group I mGlu receptor subtype 1 (pKB = 3.4 for mGlu1a). Complete absence of interacting with on group II or III mGluRs, or ionotropic glutamate receptors. Widely used in studying neural plasticity, learning and memory, and fear conditioning. Centrally active following systemic administration in vivo.
Form
Off-white powder
CAS number
168560-79-0
Chemical formula
C₁₁H₁₁NO₄
Structure formula
Purity
≥98% by HPLC
Solubility
DMSO (2 mg/ml)
Storage
Protect from light
+15°C to +30°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
Pellicciari, R., et al. 1995. J. Med. Chem.38, 3717. Moroni, F., et al. 1997. J. Pharmacol. Exp. Ther.281, 721. Nielsen, K., et al. 1997. Eur. J. Pharmacol.326, 105.
Christoffersen, G., et al. 1999, Neuropharmacology.38, 817.
