Date published: 2025-11-30

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Chromeo™ P429

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Application:
Chromeo™ P429 is an easy-to-use amine-reactive pyrylium dye
Molecular Weight:
369.82
Molecular Formula:
C16H16NOS•ClO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Chromeo™ P429 detects proteins and peptides by exhibiting a color change. After binding to primary amines, it undergoes a large shortwave spectral shift of 28nm that is visible to the naked eye. There is also a large increase in quantum yield that changes the non- or only weakly fluorescent dye into a bright fluorescent conjugate. The shift of the absorption & emission bands together with the increased fluorescence quantum yield effectively eliminates background from any unbound dye. In addition, because unbound the pyrylium dye is hydrolyzed during the labeling procedure, there is no need for purification following the simple one-step, room-temperature incubation. The labeled protein is ready to use immediately, and any possible background from the unbound dye is eliminated. Due to the unique conjugation mechanism, proteins labeled with Py-Dyes maintain their native charge and isoelectric point. Because of these specific features, Chromeo Py-Dyes have been used successfully in a number of "no-wash" applications such as capillary electrophoresis, SDS-protein gel electrophoresis, isoelectric focusing, and as a label in receptor binding studies.


Chromeo™ P429 References

  1. Determination of picomolar concentrations of proteins using novel amino reactive chameleon labels and capillary electrophoresis laser-induced fluorescence detection.  |  Craig, DB., et al. 2005. Electrophoresis. 26: 2208-13. PMID: 15880625
  2. Reaction of fluorogenic reagents with proteins II: capillary electrophoresis and laser-induced fluorescence properties of proteins labeled with Chromeo P465.  |  Swearingen, KE., et al. 2008. J Chromatogr A. 1194: 249-52. PMID: 18479693
  3. Reaction of fluorogenic reagents with proteins III. Spectroscopic and electrophoretic behavior of proteins labeled with Chromeo P503.  |  Turner, EH., et al. 2008. J Chromatogr A. 1194: 253-6. PMID: 18482729
  4. Fluorescence measurements on functionalized polymer surfaces--problems and troubleshooting.  |  Hoffmann, K., et al. 2008. Ann N Y Acad Sci. 1130: 28-34. PMID: 18596328
  5. Attomole protein analysis by CIEF with LIF detection.  |  Ramsay, LM., et al. 2009. Electrophoresis. 30: 297-302. PMID: 19204946
  6. Femtomolar concentration detection limit and zeptomole mass detection limit for protein separation by capillary isoelectric focusing and laser-induced fluorescence detection.  |  Ramsay, LM., et al. 2009. Anal Chem. 81: 1741-6. PMID: 19206532
  7. Capillary array isoelectric focusing with laser-induced fluorescence detection: milli-pH unit resolution and yoctomole mass detection limits in a 32-channel system.  |  Dada, OO., et al. 2010. Anal Bioanal Chem. 397: 3305-10. PMID: 20336452
  8. Two-dimensional capillary electrophoresis: capillary isoelectric focusing and capillary zone electrophoresis with laser-induced fluorescence detection.  |  Dickerson, JA., et al. 2010. Electrophoresis. 31: 2650-4. PMID: 20603830
  9. Red-fluorescent argininamide-type NPY Y1 receptor antagonists as pharmacological tools.  |  Keller, M., et al. 2011. Bioorg Med Chem. 19: 2859-78. PMID: 21493077
  10. Protein labeling enhances aptamer selection by methods of kinetic capillary electrophoresis.  |  de Jong, S. and Krylov, SN. 2011. Anal Chem. 83: 6330-5. PMID: 21728308
  11. Pressure-based approach for the analysis of protein adsorption in capillary electrophoresis.  |  de Jong, S. and Krylov, SN. 2012. Anal Chem. 84: 453-8. PMID: 22107082
  12. Glycan analysis via derivatization with a fluorogenic pyrylium dye.  |  Johannesen, SA., et al. 2012. Carbohydr Res. 352: 94-100. PMID: 22425443

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Chromeo™ P429, 1 mg

sc-364760
1 mg
$637.00