Product overview
| Name | p-Nitrobenzyl mesylate (PNBM) |
| Biological description | Alkylation reagent. Commonly used to tag substrates for isolation by immunoprecipitation or immunoaffinity purification or detection by immunoblotting. Alkylates thiophosphates (e.g. substrates phosphorylated with ATPgammaS or N6-benzyl-ATPgammaS) to form thiophosphate ester epitopes that can be recognized by antibodies. Prepare a 50 mM PNBM (12 mg/ml) stock by dissolving PNBM in DMSO and vortexing. |
| Description | Alkylation reagent that alkylates thiophosphates |
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Solubility & Handling
| Storage instructions | -20°C |
| Solubility overview | soluble in DMSO to 100 mM |
| Important | This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use. |
Chemical Data
| Chemical name | 4-nitro-benzenemethanol, 1-methanesulfonate |
| Molecular Weight | 231.22 |
| Molecular Formula | C8H9NO5S |
| CAS Number | 39628-94-9 |
| PubChem identifier | 18924794 |
| SMILES | CS(=O)(=O)OCC1=CC=C(C=C1)[N+](=O)[O-] |
| Source | Synthetic |
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