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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181198
Sigma-AldrichArachidonic Acid - CAS 506-32-1 - Calbiochem
Precursor for prostaglandins, prostacyclin, and thromboxane.
More>>Precursor for prostaglandins, prostacyclin, and thromboxane. Less<<
Arachidonic Acid - CAS 506-32-1 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
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Description
Overview
Precursor for prostaglandins, prostacyclin, and thromboxane. Binds to G-protein α-subunits in a covalent, post-translational manner. Inhibits Ras-GAP. Stimulates the synthesis of nitric oxide by platelets. Modulates nitric oxide production by prostaglandin synthesis via the cyclooxygenase pathway.
Arachidonic Acid - CAS 506-32-1 - Calbiochem Certificates of Analysis
Title
Lot Number
181198
References
Reference overview
Hallak, H., et al. 1994. J. Biol. Chem. 269, 4713. Khurana, G., and Bennett, M.R. 1993. Br. J. Pharmacol. 109, 480. Han, J.-W., et al. 1991. Science252, 576. Radomski, M.W., et al. 1990. Br. J. Pharmacol. 101, 325. Neddleman P., et al. 1986. Annu. Rev. Biochem.55, 69.
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 cis-polyunsaturated fatty acid found in the plasma membrane. Major component of membrane phospholipids. Following its release by cellular phospholipases, it is enzymatically converted to a variety of inflammatory and vasoactive metabolites, such as prostaglandins (via the cyclooxygenase pathway), leukotrienes (via the lipoxygenase pathway), and epoxides (via the cytochrome P450 pathway). Binds to G-protein α-subunits in a covalent, posttranslational manner. Inhibits Ras-GAP. Stimulates the synthesis of nitric oxide by platelets.
Form
Colorless oil
Intert gas (Yes/No)
Packaged under inert gas
CAS number
506-32-1
RTECS
CE6675000
Chemical formula
C₂₀H₃₂O₂
Structure formula
Purity
≥99% by TLC and GC
Solubility
Ethanol (5 mg/ml)
Storage
Protect from light ≤ -70°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
Toxicity
Harmful
Merck USA index
14, 765
References
Hallak, H., et al. 1994. J. Biol. Chem. 269, 4713. Khurana, G., and Bennett, M.R. 1993. Br. J. Pharmacol. 109, 480. Han, J.-W., et al. 1991. Science252, 576. Radomski, M.W., et al. 1990. Br. J. Pharmacol. 101, 325. Neddleman P., et al. 1986. Annu. Rev. Biochem.55, 69.