Date published: 2026-4-21

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STE buffer solution

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Application:
STE buffer solution is a sodium Chloride-Tris-EDTA buffer formulated for DNA extraction protocols. pH 7.8±0.2 (25° C)
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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STE buffer solution, an abbreviation for Sodium Chloride-Tris-EDTA buffer, is a fundamental reagent in molecular biology research, playing a pivotal role in various experimental procedures. This solution is meticulously formulated to provide a stable and controlled environment for the manipulation and analysis of nucleic acids. The mechanism of action of STE buffer relies on its composition of three key components: Sodium Chloride (NaCl), Tris, and Ethylenediaminetetraacetic acid (EDTA). NaCl maintains the ionic strength of the buffer, ensuring proper solubility of macromolecules and stabilizing interactions between biomolecules. Tris serves as a buffering agent, maintaining a constant pH in the solution, critical for enzymatic reactions and nucleic acid stability. EDTA, a chelating agent, sequesters divalent metal ions, preventing their interference with enzymatic reactions and protecting nucleic acids from degradation. In research, STE buffer solution finds widespread use in DNA and RNA extraction, purification, and storage. It facilitates cell lysis, solubilization of nucleic acids, and maintains their integrity during experimental procedures such as gel electrophoresis, polymerase chain reaction (PCR), and restriction enzyme digestion. Furthermore, STE buffer is an essential component of various commercial kits used for nucleic acid isolation and analysis, contributing to its indispensable role in molecular biology laboratories worldwide. Ongoing research endeavors continue to explore innovative applications and optimizations of STE buffer formulations, advancing nucleic acid research, diagnostics, and biotechnology.


STE buffer solution References

  1. Electrical detection of deoxyribonucleic acid hybridization based on carbon-nanotubes/nano zirconium dioxide/chitosan-modified electrodes.  |  Yang, Y., et al. 2007. Anal Chim Acta. 584: 268-74. PMID: 17386614
  2. Size and mechanical stability of norovirus capsids depend on pH: a nanoindentation study.  |  Cuellar, JL., et al. 2010. J Gen Virol. 91: 2449-56. PMID: 20592107
  3. Safer DNA extraction from plant tissues using sucrose buffer and glass fiber filter.  |  Takakura, K. and Nishio, T. 2012. J Plant Res. 125: 805-7. PMID: 22695723
  4. Evaluation of real-time PCR for quantitative detection of Escherichia coli in beach water.  |  Lam, JT., et al. 2014. J Water Health. 12: 51-6. PMID: 24642432
  5. Physiology at near-critical temperatures, but not critical limits, varies between two lizard species that partition the thermal environment.  |  Telemeco, RS., et al. 2017. J Anim Ecol. 86: 1510-1522. PMID: 28796906
  6. A complete species-level phylogeny of the Erythrura parrotfinches (Aves: Estrildidae).  |  DeCicco, LH., et al. 2023. Mol Phylogenet Evol. 187: 107883. PMID: 37481145
  7. Accumulation of replicative intermediates of mitochondrial DNA in Tetrahymena pyriformis grown in ethidium bromide.  |  Upholt, WB. and Borst, P. 1974. J Cell Biol. 61: 383-97. PMID: 4208072
  8. Bovine enterovirus-1: characterization, replication and cytopathogenic effects.  |  Taylor, MW., et al. 1974. J Gen Virol. 23: 173-8. PMID: 4364878
  9. Suggestive evidence for an oncorna-virus-specific DNA polymerase from C-type particles of bovine leukosis.  |  Dietzschold, B., et al. 1974. Z Naturforsch C Biosci. 29: 72-5. PMID: 4367192
  10. An analysis of analyte-receptor binding kinetics for biosensor applications: influence of the fractal dimension on the binding rate coefficient.  |  Sadana, A. 1998. Biosens Bioelectron. 13: 1127-40. PMID: 9842708

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

STE buffer solution, 100 ml

sc-296422
100 ml
$46.00

STE buffer solution, 500 ml

sc-296422A
500 ml
$154.00