Date published: 2026-5-4

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MOPS/EDTA Buffer, 10X Liquid Concentrate

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Application:
MOPS/EDTA Buffer, 10X Liquid Concentrate is a buffer for RNA electrophoresis in denaturing (formaldehyde) agarose gels
Molecular Weight:
209.26
Molecular Formula:
C7H15NO4S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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MOPS/EDTA buffer, in its 10X liquid concentrate form, is a vital component in various biochemical and molecular biology research applications. MOPS, or 3-(N-morpholino)propanesulfonic acid, serves as the buffering agent in this solution, while EDTA (ethylenediaminetetraacetic acid) acts as a chelating agent. In research, buffers play a critical role in maintaining pH stability and providing an optimal environment for biochemical reactions. MOPS is a zwitterionic buffer with a pKa near physiological pH, making it suitable for biological studies requiring precise pH control. Its chemical structure confers resistance to changes in pH caused by temperature fluctuations, ensuring the stability of experimental conditions over time. EDTA, on the other hand, functions as a chelating agent by sequestering divalent metal ions, such as magnesium (Mg^2+), which are often involved in enzymatic reactions. By chelating metal ions, EDTA prevents their interference with enzymatic activity, thereby ensuring the accuracy and reproducibility of biochemical assays. The combination of MOPS and EDTA in this buffer solution provides researchers with a versatile tool for various applications, including nucleic acid electrophoresis, protein biochemistry, and enzyme assays. Its compatibility with a wide range of experimental conditions and its ability to maintain stable pH make MOPS/EDTA buffer indispensable in biochemical and molecular biology laboratories, facilitating reliable and reproducible research outcomes.


MOPS/EDTA Buffer, 10X Liquid Concentrate References

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  2. Spin labeled cysteines as sensors for protein-lipid interaction and conformation in rhodopsin.  |  Farahbakhsh, ZT., et al. 1992. Photochem Photobiol. 56: 1019-33. PMID: 1492127
  3. Purification and phosphorylation of the Arc regulatory components of Escherichia coli.  |  Iuchi, S. and Lin, EC. 1992. J Bacteriol. 174: 5617-23. PMID: 1512197
  4. Development of a Plexor real-time PCR assay for the detection of porcine circovirus type 2.  |  Vlasakova, M., et al. 2012. J Virol Methods. 179: 311-5. PMID: 22155430
  5. Detection and identification of Phoma pathogens of potato.  |  A'Hara, D. 2015. Methods Mol Biol. 1302: 17-27. PMID: 25981243
  6. Constitutive production of interleukin-8 (IL-8) by normal and malignant human B-cells and other cell types.  |  Srivastava, MD., et al. 1993. Leuk Res. 17: 1063-9. PMID: 8246610
  7. Expression of apolipoprotein A-I in porcine brain endothelium in vitro.  |  Möckel, B., et al. 1994. J Neurochem. 62: 788-98. PMID: 8294940
  8. Muscarinic acetylcholine receptor-mediated induction of zif268 mRNA in PC12D cells requires protein kinase C and the influx of extracellular calcium.  |  Ebihara, T. and Saffen, D. 1997. J Neurochem. 68: 1001-10. PMID: 9048745
  9. Characterization of glucose-6-phosphate-dependent glycogen synthase from Dictyostelium discoideum.  |  Saunders, et al. 1977. Microbiology. 100.1: 89-97.
  10. with chloroplasts in tobacco.  |  Gunasinghe, U. and P. H. Berger. 1991. Mol Plant Microbe Interact. 4.5: 452-457.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

MOPS/EDTA Buffer, 10X Liquid Concentrate, 100 ml

sc-286313
100 ml
$55.00