Phos-tag™ Phosphorylation Reagent
The Phos-tag™ developed by Hiroshima University is a functional molecule that binds phosphorylated ions, forming stable complexes under physiological conditions. This has been used to develop a range of products to assist the study of phosphorylation.

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Phos-tag™ Acrylamide
Phos-tag acrylamide can be used for mobility shift detection of phosphorylated proteins using phosphate affinity SDS-PAGE. Phos-tag labelled acrylamide is incorporated into the gel and subsequently during electrophoresis serves to retard the progress of phosphorylated proteins through the gel enabling separation of phosphorylated and non-phosphorylated isomers.
Phos-tag™ Agarose
Phos-tag™ agarose can be used to construct a phosphate affinity column enabling purification of phosphorylated proteins suitable for down-stream analysis such as mass spectrometry or SDS-PAGE.
Phos-tag™ Biotin
Phos-tag™ biotin ligands can be used to detect phosphorylated proteins on PVDF membrane as an alternative to anti-phosphorylated antibodies. Unlike traditional immunodetection the membranes can be probed without blocking and phos-tag biotin is sensitive enough to detect phosphorylated protein at nanogram levels.Subsequently membranes can easily be stripped and reprobed with conventional antibodies if desired.
Mass Spectrometry Kit
The Phos-tag™ mass analytical kit can be used to provide rapid and sensitive matrix-assisted laser desorption/ionisation-time of flight mass spectrometry using natural zinc and stable isotopes 64Zn and 68Zn.
Brochures
Phos-tag™ Tool Kit: Protein phosphorylation analysis - radiation free
This product brochure introduces Phos-tag™, a functional molecule that binds phosphorylated ions to form stable complexes under physiological conditions. Developed by the Department of Functional Molecular Science at Hiroshima University, Phos-tag™ has an affinity for the phosphate dianion, PO42-, which is much higher than that for other negative ions, leading to its selectivity. Phos-tag™ can take the place of conventional enzyme immunoassay and radioactive isotope methods as an agent for capturing substances with a phosphate monoester group in phosphorylation analysis techniques.








