TAE Buffer – High-Performance Electrophoresis Solution for DNA & RNA Separation
TAE buffer (Tris-Acetate-EDTA) is a widely used electrophoresis buffer in molecular biology laboratories, ensuring efficient DNA and RNA separation in agarose gel electrophoresis. IBI Scientific’s 10X TAE Buffer provides a reliable, high-quality solution that delivers faster migration of double-stranded DNA compared to TBE buffer. With its ability to resolve supercoiled DNA with superior clarity, TAE buffer is a preferred choice for researchers conducting low-voltage DNA electrophoresis experiments.
While TAE buffer’s buffering capacity can become exhausted during extended or high-voltage runs, it remains the ideal choice for high-resolution applications where precise DNA separation is essential. This 10X concentrated solution allows users to prepare up to 10 liters of 1X TAE buffer, ensuring flexibility and efficiency in laboratory workflows.
Why Choose IBI Scientific's 10X TAE Buffer?
- Superior DNA migration – Faster movement of double-stranded DNA than TBE buffer.
- Excellent resolution – Ideal for supercoiled, linear, and circular DNA.
- Flexible preparation – Dilutes to 1X for up to 10 liters of working solution.
- Reliable separation – Ensures DNA integrity and reproducibility in agarose gel electrophoresis.
- High purity – Made with molecular biology-grade Tris, Acetate, and EDTA.
Optimized for Electrophoresis Performance
IBI Scientific’s TAE buffer is an essential electrophoresis reagent, delivering reliable, high-quality results in molecular biology research. Designed for superior DNA migration, it ensures accurate, reproducible nucleic acid separations with high-resolution clarity.
Upgrade your lab with IBI Scientific’s 10X TAE Buffer today and achieve superior DNA electrophoresis results!
FAQs: Everything You Need to Know About TAE Buffer
TAE buffer (Tris-Acetate-EDTA) is a buffering solution used in DNA and RNA electrophoresis to maintain a stable pH environment and enhance nucleic acid mobility in agarose gels. It prevents nucleic acids from degrading while facilitating efficient separation based on size.
Unlike water, TAE buffer conducts electricity and maintains a stable pH throughout the electrophoresis process. Using water would result in rapid pH fluctuations, poor DNA mobility, and ineffective separation of nucleic acids.
While both contain Tris and EDTA, they serve different purposes:
- TAE buffer is designed for DNA and RNA electrophoresis, ensuring optimal separation in gels.
- TE buffer (Tris-EDTA) is used for DNA and RNA storage, protecting nucleic acids from degradation.
