Date published: 2026-5-4

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Tris Acetate-EDTA buffer, 10X

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Application:
Tris Acetate-EDTA buffer, 10X is prepared with high-quality reagents for DNA or non-denaturing RNA agarose gel electrophoresis
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tris Acetate-EDTA (TAE) buffer, 10X concentration, is a vital reagent in molecular biology research, particularly in nucleic acid electrophoresis and analysis. This concentrated buffer solution is meticulously formulated to provide optimal conditions for the separation and visualization of DNA and RNA fragments on agarose gels. In research, 10X TAE buffer is commonly diluted to a working concentration (typically 1X or 0.5X) for use in agarose gel electrophoresis. This concentrated form allows for flexibility in experimental design and reduces the volume of buffer required for gel preparation, saving time and resources. Additionally, 10X TAE buffer provides enhanced buffering capacity and conductivity, facilitating efficient nucleic acid migration and sharper band resolution during electrophoresis. Furthermore, 10X TAE buffer is compatible with various nucleic acid stains and visualization methods, allowing researchers to accurately detect and analyze DNA and RNA fragments following electrophoresis. It is an essential component in techniques such as restriction fragment length polymorphism (RFLP) analysis, DNA fragment sizing, and nucleic acid purification from agarose gels. Ongoing research efforts focus on further optimizing the formulation and concentration of TAE buffer for specific applications, as well as exploring its compatibility with emerging nucleic acid analysis technologies.


Tris Acetate-EDTA buffer, 10X References

  1. Improvements in gel composition and electrophoretic conditions for broad-range mutation analysis by denaturing gradient gel electrophoresis.  |  Hayes, VM., et al. 1999. Nucleic Acids Res. 27: e29. PMID: 10497279
  2. Capillary electrophoresis of DNA in the 20-500 bp range: recent developments.  |  Righetti, PG. and Gelfi, C. 1999. J Biochem Biophys Methods. 41: 75-90. PMID: 10626767
  3. The free solution mobility of DNA in Tris-acetate-EDTA buffers of different concentrations, with and without added NaCl.  |  Stellwagen, E. and Stellwagen, NC. 2002. Electrophoresis. 23: 1935-41. PMID: 12116139
  4. History and principles of conductive media for standard DNA electrophoresis.  |  Brody, JR. and Kern, SE. 2004. Anal Biochem. 333: 1-13. PMID: 15351274
  5. Electrophoresis of DNA in agarose gels, polyacrylamide gels and in free solution.  |  Stellwagen, NC. 2009. Electrophoresis. 30 Suppl 1: S188-95. PMID: 19517510
  6. Electrophoresis in agarose and acrylamide gels.  |  Ogden, RC. and Adams, DA. 1987. Methods Enzymol. 152: 61-87. PMID: 2443811
  7. Semi-Automatic Lab-on-PCB System for Agarose Gel Preparation and Electrophoresis for Biomedical Applications.  |  Urbano-Gámez, JD., et al. 2021. Micromachines (Basel). 12: PMID: 34577715
  8. The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis.  |  Loening, UE. 1967. Biochem J. 102: 251-7. PMID: 5339944
  9. Recent advances in capillary zone electrophoresis of DNA.  |  Righetti, PG. and Gelfi, C. 1998. Forensic Sci Int. 92: 239-50. PMID: 9627982
  10. Apparent pore size of polyacrylamide gels: comparison of gels cast and run in Tris-acetate-EDTA and Tris-borate-EDTA buffers.  |  Stellwagen, NC. 1998. Electrophoresis. 19: 1542-7. PMID: 9719523

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tris Acetate-EDTA buffer, 10X, 100 ml

sc-296647
100 ml
$9.00

Tris Acetate-EDTA buffer, 10X, 1 L

sc-296647A
1 L
$37.00