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Tris-Borate-EDTA buffer, 5X (CAS 610769-35-2)

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Application:
Tris-Borate-EDTA buffer, 5X is a concentrated solution ready to use for DNA and RNA polyacrylamide gel electrophoresis
CAS Number:
610769-35-2
Molecular Weight:
475.21
Molecular Formula:
C14H30BN3O14
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-Borate-EDTA (TBE) buffer, in its 5X concentrated form, is a crucial reagent extensively employed 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, visualization, and analysis of nucleic acid fragments on agarose or polyacrylamide gels. In research, 5X TBE buffer is commonly diluted to a working concentration (typically 1X) 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, 5X TBE buffer provides enhanced buffering capacity and conductivity, resulting in sharp and well-resolved nucleic acid bands during electrophoresis. Furthermore, 5X TBE 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 TBE buffer for specific applications, as well as exploring its compatibility with emerging nucleic acid analysis technologies.


Tris-Borate-EDTA buffer, 5X (CAS 610769-35-2) References

  1. DNA and buffers: are there any noninteracting, neutral pH buffers?  |  Stellwagen, NC., et al. 2000. Anal Biochem. 287: 167-75. PMID: 11078596
  2. Effects of polyols, pH and electrolyte concentrations in TBE buffer on separation of double strand DNA fragments by capillary electrophoresis.  |  Ren, J., et al. 2002. Anal Sci. 18: 469-71. PMID: 11999525
  3. Sequence-specific and nonspecific mobilities of single-stranded oligonucleotides observed by changing the borate buffer concentration.  |  Biyani, M. and Nishigaki, K. 2003. Electrophoresis. 24: 628-33. PMID: 12601730
  4. THE AMINO ACID COMPOSITION OF HEMOGLOBIN. V. THE PREPARATION OF PURIFIED HEMOGLOBIN FRACTIONS BY CHROMATOGRAPHY ON CELLULOSE EXCHANGERS AND THEIR IDENTIFICATION BY STARCH GEL ELECTROPHORESIS USING TRIS-BORATE-EDTA BUFFER.  |  CHERNOFF, AI., et al. 1965. Blood. 25: 646-61. PMID: 14282035
  5. Electrophoretic separation of DNA using a new matrix in uncoated capillaries.  |  Zhou, P., et al. 2005. J Chromatogr A. 1083: 173-8. PMID: 16078704
  6. Effect of buffer flow on DNA separation in a microfabricated electrophoresis system.  |  Chen, Z. and Burns, MA. 2005. Electrophoresis. 26: 4718-28. PMID: 16294296
  7. Discontinuous buffer system for polyacrylamide and agarose gel electrophoresis of DNA fragments.  |  Orbán, L. and Chrambach, A. 1991. Electrophoresis. 12: 233-40. PMID: 2070779
  8. Glycoprotein molecular-weight estimation using sodium dodecyl sulfate-pore gradient electrophoresis: comparison of tris-glycine and tris-borate-EDTA buffer systems.  |  Poduslo, JF. 1981. Anal Biochem. 114: 131-9. PMID: 6169294
  9. SDS agarose gels for analysis of proteins.  |  Wu, M. and Kusukawa, N. 1998. Biotechniques. 24: 676-8. PMID: 9564543
  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-Borate-EDTA buffer, 5X, 4 L

sc-296652
4 L
$48.00