Date published: 2026-4-4

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Tris-Phosphate-EDTA Buffer 10X

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Alternate Names:
TPE Buffer
Application:
Tris-Phosphate-EDTA Buffer 10X is concentrate for use in gel electrophoresis following dilution to working concentrations
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-Phosphate-EDTA (TPE) buffer, in its 10X concentrated form, is a crucial reagent extensively employed in molecular biology research, particularly in nucleic acid electrophoresis and DNA/RNA gel analysis. This concentrated buffer solution is meticulously formulated to provide optimal conditions for the separation, visualization, and analysis of nucleic acid fragments on agarose or polyacrylamide gels. In research, 10X TPE buffer is commonly diluted to a working concentration (typically 1X or 0.5X) for use in agarose or polyacrylamide 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 TPE buffer provides enhanced buffering capacity and conductivity, resulting in sharp and well-resolved nucleic acid bands during electrophoresis. Furthermore, 10X TPE buffer is compatible with various nucleic acid stains and visualization methods, enabling the accurate detection and analysis of 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 TPE buffer for specific applications, as well as exploring its compatibility with emerging nucleic acid analysis technologies.


Tris-Phosphate-EDTA Buffer 10X References

  1. DNA separation by capillary electrophoresis with hydrophilic substituted celluloses as coating and sieving polymers. Application to the analysis of genetically modified meals.  |  Giovannoli, C., et al. 2004. J Sep Sci. 27: 1551-6. PMID: 15638166
  2. Factors affecting the extraction of intact ribonucleic Acid from plant tissues containing interfering phenolic compounds.  |  Newbury, HJ. and Possingham, JV. 1977. Plant Physiol. 60: 543-7. PMID: 16660134
  3. Purification and mapping of specific mRNAs by hybridization-selection and cell-free translation.  |  Ricciardi, RP., et al. 1979. Proc Natl Acad Sci U S A. 76: 4927-31. PMID: 291909
  4. An intragenic deletion of the factor IX gene in a family with hemophilia B.  |  Chen, SH., et al. 1985. J Clin Invest. 76: 2161-4. PMID: 3001143
  5. Gel electrophoresis of RNA under denaturing conditions.  |  Reijnders, L., et al. 1973. Biochim Biophys Acta. 324: 320-33. PMID: 4202717
  6. Hormonal control of alpha-amylase gene expression in barley. Studies using a cloned CDNA probe.  |  Muthukrishnan, S., et al. 1983. J Biol Chem. 258: 2370-5. PMID: 6185494
  7. Knotting of the circular duplex DNA by type II DNA topoisomerase from Drosophila melanogaster.  |  Hsieh, T. 1983. J Biol Chem. 258: 8413-20. PMID: 6305983
  8. Genes involved in the virulence of an avian influenza virus.  |  Ogawa, T. and Ueda, M. 1981. Virology. 113: 304-13. PMID: 7269245
  9. Analysis of restriction fragments of T7 DNA and determination of molecular weights by electrophoresis in neutral and alkaline gels.  |  McDonell, MW., et al. 1977. J Mol Biol. 110: 119-46. PMID: 845942

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tris-Phosphate-EDTA Buffer 10X, 1 L

sc-296655
1 L
$176.00