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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506419
Sigma-AldrichMethysergide Maleate - CAS 129-49-7 - Calbiochem
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Description
Overview
An antagonist of the 5-HT2B (pki = 8.0-9.4) and 5-HT2C (pki = 8.6-9.1) receptor. At the 5-HT1A and some other 5-HT receptors it serves as a partial agonist. It is known to have partial agonist effects on other 5-HT receptors as well. In neuronal and platelet culture, Methysergide blocks serotonin action with an IC50 = 18 µM. Originally developed in the 1960′s as a migraine/cluster headache treatment, but discontinued due to significant physiological and pyschotropic side effects. Methysergide is still actively used in research as a 5-HT2 receptor antagonist in both in vivo and in vitro experiments.
Wear suitable protective clothing, gloves and eye/face protection. If swallowed, seek medical advice immediately and show this container or label.
Storage and Shipping Information
Ship Code
Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Toxicity
Toxic
Hazardous Materials Attention:
Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
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.
Global Trade Item Number
Catalogue Number
GTIN
5064190001
04055977242737
Documentation
Methysergide Maleate - CAS 129-49-7 - Calbiochem SDS
Matsuta, Y. et al. 2013. Exp. Neurol.247, 250. IUHPAR Database 2013. Shad, K.F., Saeed, S.A. 2007. Exp. Brain Res.183, 411. Knight, A.R. et al. 2004. Naunyn Schmiedebergs Arch. Pharmacol.370, 114. Saxena, P.R and Lawang, A. 1985. Arch. Int. Pharmacodyn. Ther.277, 235. Colpaert, F. C. et al. 1979. Eur. J. Pharmacol.58, 505.
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.
An antagonist of the 5-HT2B (pki = 8.0-9.4) and 5-HT2C (pki = 8.6-9.1) receptor. At the 5-HT1A and some other 5-HT receptors it serves as a partial agonist. It is known to have partial agonist effects on other 5-HT receptors as well. In neuronal and platelet culture, Methysergide blocks serotonin action with an IC50 = 18 µM. Originally developed in the 1960′s as a migraine/cluster headache treatment, but discontinued due to significant physiological and pyschotropic side effects. Methysergide is still actively used in research as a 5-HT2 receptor antagonist in both in vivo and in vitro experiments.
Form
Off-white solid
CAS number
129-49-7
Chemical formula
C₂₁H₂₇N₃O₂·C₄H₄O₄
Structure formula
Purity
≥99% by HPLC
Solubility
H₂O (10 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
Toxic
References
Matsuta, Y. et al. 2013. Exp. Neurol.247, 250. IUHPAR Database 2013. Shad, K.F., Saeed, S.A. 2007. Exp. Brain Res.183, 411. Knight, A.R. et al. 2004. Naunyn Schmiedebergs Arch. Pharmacol.370, 114. Saxena, P.R and Lawang, A. 1985. Arch. Int. Pharmacodyn. Ther.277, 235. Colpaert, F. C. et al. 1979. Eur. J. Pharmacol.58, 505.
