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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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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505881
Sigma-Aldrich(R)-(+)-SKF38393 Hydrochloride - CAS 81702-42-3 - Calbiochem
A benzazepine derivative that acts as a selective Dopamine D1/D5 receptor partial agonist. Examination of the isomers in several in vitro and in vivo tests for both central and peripheral dopaminergic activity revealed that activity resided almost exclusively in the R isomer. The results suggest that the properly oriented 1-phenyl substituent of 1 is important for dopamine-like activity. Reported to have stimulant and anorectic effects.
Trampus, M. et al. 1993. J. Pharmacol.235, 83. Cooper, S. J. et al. 1990. Psychopharmacol.100, 182. Dubois, A. et al. 1986. Neurosci.19, 125. Kaiser, C. C. et al. 1982. J. Med. Chem.25, 697.
Trampus, M. et al. 1993. J. Pharmacol.235, 83. Cooper, S. J. et al. 1990. Psychopharmacol.100, 182. Dubois, A. et al. 1986. Neurosci.19, 125. Kaiser, C. C. et al. 1982. J. Med. Chem.25, 697.
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.
A benzazepine derivative that acts as a selective Dopamine D1/D5 receptor partial agonist. Examination of the isomers in several in vitro and in vivo tests for both central and peripheral dopaminergic activity revealed that activity resided almost exclusively in the R isomer. The results suggest that the properly oriented 1-phenyl substituent of 1 is important for dopamine-like activity. Reported to have stimulant and anorectic effects.
Form
White solid
CAS number
81702-42-3
Chemical formula
C16H₁₇NO₂•HCl
Structure formula
Purity
≥98% by HPLC
Solubility
H₂O (100 mM)
Storage
Protect from light -20°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
Trampus, M. et al. 1993. J. Pharmacol.235, 83. Cooper, S. J. et al. 1990. Psychopharmacol.100, 182. Dubois, A. et al. 1986. Neurosci.19, 125. Kaiser, C. C. et al. 1982. J. Med. Chem.25, 697.
