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
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-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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584222
MilliporeTetrahydrouridine - CAS 18771-50-1 - Calbiochem
Potent competitive inhibitor of cytidine deaminase. Also available as a 100 mM solution in H2O.
More>>Potent competitive inhibitor of cytidine deaminase. Also available as a 100 mM solution in H2O. Less<<
MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
Following reconstitution, aliquot, purge with inert gas, and freeze (-20°C). Aqueous stock solutions (at neutral or basic pH) are stable for up to 3 months at -20°C.
Packaging Information
Packaged under inert gas
Packaged under inert gas
Global Trade Item Number
Catalogue Number
GTIN
584222-10MG
04055977264944
Documentation
Tetrahydrouridine - CAS 18771-50-1 - Calbiochem SDS
Tetrahydrouridine - CAS 18771-50-1 - Calbiochem Certificates of Analysis
Title
Lot Number
584222
References
Reference overview
Yusa, K., et al. 1995. Biochem. Biophys. Res. Commun. 206, 486. Bouffard, D.Y., et al. 1993. Biochem Pharmacol.45, 1857. Laliberte, J., et al. 1992. Cancer Chemotherap. Pharmacol.30, 7. Riva, C., et al. 1992. Chemotherapy38, 358. Yusa, K., et al. 1992. J. Biol. Chem. 267, 16848. Hanze, A.R. 1967. J. Am. Chem. Soc.89, 6720.
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
21-June-2013 JSW
Description
A potent competitive inhibitor of cytidine deaminase. Used in combination with cytosine arabinoside (Ara-C) to assess the anti-leukemic activity and anti-tumor activity of Ara-C in in vitro studies.
Form
White to off-white solid
Intert gas (Yes/No)
Packaged under inert gas
CAS number
18771-50-1
RTECS
UW5798980
Chemical formula
C₉H₁₆N₂O₆
Purity
≥90% by TLC
Solubility
H₂O (200 mg/ml)
Storage
Protect from light -20°C Hygroscopic
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot, purge with inert gas, and freeze (-20°C). Aqueous stock solutions (at neutral or basic pH) are stable for up to 3 months at -20°C.
Toxicity
Standard Handling
References
Yusa, K., et al. 1995. Biochem. Biophys. Res. Commun. 206, 486. Bouffard, D.Y., et al. 1993. Biochem Pharmacol.45, 1857. Laliberte, J., et al. 1992. Cancer Chemotherap. Pharmacol.30, 7. Riva, C., et al. 1992. Chemotherapy38, 358. Yusa, K., et al. 1992. J. Biol. Chem. 267, 16848. Hanze, A.R. 1967. J. Am. Chem. Soc.89, 6720.
