Date published: 2026-3-31

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Running Buffer, 10X

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Application:
Running Buffer, 10X is Tris-Glycine WB Running Buffer, pH 8.3; for sodium dodecyl sulfate – polyacrylamide gel electrophoresis (SDS-PAGE)
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Running Buffer, 10X, is a crucial component in various laboratory techniques, particularly in the realm of molecular biology and biochemistry research. Comprising a precisely balanced mixture of ions and buffering agents, this solution serves as a medium for conducting electrophoresis experiments. Its primary function is to maintain a stable pH environment, crucial for the separation of biomolecules such as DNA, RNA, and proteins based on their size and charge. In electrophoresis, Running Buffer, 10X, facilitates the migration of charged molecules through a gel matrix when an electric field is applied. The buffer′s ions conduct electricity, creating the necessary current for molecular movement. Moreover, its buffering capacity ensures that pH fluctuations are minimized during the process, thereby preserving the integrity of the samples. Research involving Running Buffer, 10X, often focuses on optimizing electrophoretic conditions for specific applications. Scientists explore various parameters, including buffer composition, voltage, and gel concentration, to achieve optimal separation and resolution of biomolecules. Additionally, studies delve into the development of novel buffer formulations to enhance electrophoretic performance, such as reducing running times or improving band sharpness. Furthermore, Running Buffer, 10X, finds utility in diverse molecular biology techniques beyond electrophoresis, such as nucleic acid blotting and capillary electrophoresis. Its precise composition and reliable performance make it an indispensable tool for researchers aiming to analyze and characterize biomolecules with high accuracy and efficiency.


Running Buffer, 10X References

  1. Running-buffer composition influences DNA-protein and protein-protein complexes detected by electrophoretic mobility-shift assay (EMSA).  |  Roder, K. and Schweizer, M. 2001. Biotechnol Appl Biochem. 33: 209-14. PMID: 11389675
  2. Competitive immunoassay for vancomycin using capillary electrophoresis with laser-induced fluorescence detection.  |  Lam, MT. and Le Chris, X. 2002. Analyst. 127: 1633-7. PMID: 12537372
  3. Capturing SDS-treated biotinylated protein and peptide by avidin functional affinity electrophoresis with or without SDS in the gel running buffer.  |  Lee, BS., et al. 2005. Anal Biochem. 336: 312-5. PMID: 15620898
  4. Models of protein modification in Tris-glycine and neutral pH Bis-Tris gels during electrophoresis: effect of gel pH.  |  Hachmann, JP. and Amshey, JW. 2005. Anal Biochem. 342: 237-45. PMID: 15935323
  5. Gel mobility shift assays to detect protein-RNA interactions.  |  Yakhnin, AV., et al. 2012. Methods Mol Biol. 905: 201-11. PMID: 22736005
  6. Screening for protein-protein interactions with asymmetrical flow field-flow fractionation.  |  Wahlund, PO., et al. 2021. J Pharm Sci. 110: 2336-2339. PMID: 33640337
  7. Out-of-Equilibrium Measurements of Kinetic Constants on a Biosensor.  |  Mottin, D., et al. 2021. Anal Chem. 93: 7266-7274. PMID: 33960190
  8. The gradient-like separation and reduced running time with Tris-Tricine-HEPES buffer for SDS-PAGE.  |  Dumut, DC., et al. 2022. Anal Biochem. 653: 114789. PMID: 35738440
  9. The number of neurophysins in the rat. Influence of the concentration of Bromophenol Blue, used as a tracking dye, on the resolution of proteins by polyacrylamide-gel electrophoresis.  |  Burford, GD. and Pickering, BT. 1972. Biochem J. 128: 941-4. PMID: 4638797
  10. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.  |  Laemmli, UK. 1970. Nature. 227: 680-5. PMID: 5432063

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Running Buffer, 10X, 1 L

sc-24949
1 L
$33.00