Date published: 2026-4-11

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Coomassie Stain

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Application:
Coomassie Stain is used to stain proteins in SDS-PAGE gels.
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Coomassie Stain, commonly referred to as Coomassie Brilliant Blue, is a family of dyes used extensively in biochemical research for the purpose of staining proteins in gel electrophoresis applications, such as SDS-PAGE. The dye binds to proteins non-specifically, primarily through interactions with basic amino acids (arginine, lysine) and non-polar residues in the proteins, which results in the intense blue coloration of the protein bands against a clear or lightly stained background. This staining mechanism is based on the van der Waals forces and hydrogen bonding between the dye molecules and the protein. Coomassie Stain is available in two major formulations: Coomassie Brilliant Blue R-250 and G-250. R-250 is known for producing more intense and sharper staining but requires a methanol-acetic acid-water solution for destaining, while G-250, used in the colloidal form, provides more sensitive staining and requires less toxic solvents for destaining. In research applications, Coomassie staining is valued for its simplicity, cost-effectiveness, and relatively quick process, allowing for the visualization of protein purity and the approximate quantification of protein concentration in samples. The stain′s ability to provide rapid feedback on the efficacy of protein extraction and purification processes makes it an indispensable tool in molecular biology laboratories.


Coomassie Stain References

  1. Initial analysis of the phosphoproteome of Chinese hamster ovary cells using electrophoresis.  |  Chen, Z., et al. 2004. J Biomol Tech. 15: 249-56. PMID: 15585821
  2. Suppression of human selenium-binding protein 1 is a late event in colorectal carcinogenesis and is associated with poor survival.  |  Kim, H., et al. 2006. Proteomics. 6: 3466-76. PMID: 16645984
  3. Talin-dependent integrin activation is required for fibrin clot retraction by platelets.  |  Haling, JR., et al. 2011. Blood. 117: 1719-22. PMID: 20971947
  4. Lipid, detergent, and Coomassie Blue G-250 affect the migration of small membrane proteins in blue native gels: mitochondrial carriers migrate as monomers not dimers.  |  Crichton, PG., et al. 2013. J Biol Chem. 288: 22163-73. PMID: 23744064
  5. Coomassie blue as a near-infrared fluorescent stain: a systematic comparison with Sypro Ruby for in-gel protein detection.  |  Butt, RH. and Coorssen, JR. 2013. Mol Cell Proteomics. 12: 3834-50. PMID: 24043422
  6. A one-step, low background coomassie staining procedure for polyacrylamide gels.  |  Zehr, BD., et al. 1989. Anal Biochem. 182: 157-9. PMID: 2481413
  7. A Simple, Time-Saving Dye Staining of Proteins in Sodium Dodecyl Sulfate-Polyacrylamide Gel Using Coomassie Blue.  |  Dong, WH., et al. 2018. Methods Mol Biol. 1853: 31-35. PMID: 30097927
  8. Structure of the receptor for platelet-derived growth factor helps define a family of closely related growth factor receptors.  |  Yarden, Y., et al. Nature. 323: 226-32. PMID: 3020426
  9. Production and Purification of Cysteine-Rich Leptospiral Virulence-Modifying Proteins with or Without mCherry Fusion.  |  Chaurasia, R., et al. 2023. Protein J. 42: 792-801. PMID: 37653175
  10. Properties of alpha-crystallin bound to lens membrane: probing organization at the membrane surface.  |  Chandrasekher, G. and Cenedella, RJ. 1997. Exp Eye Res. 64: 423-30. PMID: 9196394

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Coomassie Stain, 500 ml

sc-294100
500 ml
$66.00