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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:
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48-602MAG
Buffer Detection Kit for Magnetic Beads
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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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505877
Sigma-Aldrich(S)-(-)-Raclopride - CAS 84225-95-6 - Calbiochem
D2-like dopamine receptor antagonist targeting D2R (pKi =8.0), D3R (pKi = 7.9), and 5-HT1A R (pKi=5.2). Used to explore D2 like receptor mediated effects in neuropathic pain, and in antagonism studies of DA receptors during heroin usage and cocaine. D2 Receptor selectivity in various preps shows IC50 values around 32 nM.
(S)-(-)-Raclopride - CAS 84225-95-6 - Calbiochem Certificates of Analysis
Title
Lot Number
505877
References
Reference overview
Dang, Y. H. et al. 2010. Neurosci.169, 1872. Platt, D. M. et al. 2010. J. Pharmacol. Exp. Ther.332, 985.
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.
D2-like dopamine receptor antagonist targeting D2R (pKi =8.0), D3R (pKi = 7.9), and 5-HT1A R (pKi=5.2). Used to explore D2 like receptor mediated effects in neuropathic pain, and in antagonism studies of DA receptors during heroin usage and cocaine. D2 Receptor selectivity in various preps shows IC50 values around 32 nM.
Form
Off-white solid
CAS number
84225-95-6
Chemical formula
C₁₅H₂₀Cl₂N₂O₃
Structure formula
Purity
≥98% by HPLC
Solubility
DMSO (100 mM) or Ethanol (25 mM)
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
Dang, Y. H. et al. 2010. Neurosci.169, 1872. Platt, D. M. et al. 2010. J. Pharmacol. Exp. Ther.332, 985.
