1 | Cast a 1% agarose gel in 1× TAFE gel buffer (20 mM Tris-acetate (pH 8.2), 0.5 mM EDTA) without ethidium bromide and allow the gel to set. Run the gel in the same buffer solution as used for ...

In the current installment, [Justin] covers the basics of agarose gel electrophoresis ... ton of money that can be put into the things that make more sense to buy, like fluorescent DNA stain ...

The walkaway nature of the agarose gel electrophoresis systems provides substantial labor and cost savings to clinical laboratories. The semi-automated electrophoresis systems are designed for ...

No gels to pour, no buffer to make, no staining/destaining required, and no gel boxes to assemble—just load your sample and run on the E-Gel ® electrophoresis system. The major components of ...