axygen® gel documentation system

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These gels are suitable for separating nucleic acids, giving sharp DNA bands and low background fluorescence.

Explore our comprehensive portfolio of detergents and surfactants as possible Triton X-100 alternatives for your research applications before the REACH Annex 14 ban takes effect.

Amplification of DNA Using Jumpstart™ REDTaq^® DNA Polymerase (D8187)

Protocol using antibody mediated hot start polymerase with a red dye for easy gel loading. Method has short activation period (<1min), and results in higher yields and more specificity over standard PCR methods.

Determination of Caffeine in Energy Drinks with HPTLC-MS

Thin layer chromatography coupled with mass spectrometry does not require substantial sample preparation. Energy drinks can be applied without dilution directly onto the TLC plate.

Nucleic Acid Sample Preparation Methodology

Spectrophotometry can be used to estimate DNA or RNA concentration and to analyze the purity of the preparation.

Reproducibility with Biological Buffers

Biological buffers are organic substances that maintain a constant pH over a given range by neutralizing the effects of hydrogen ions.

cOmplete™ His-Tag Purification Resin Protocol & Troubleshooting

Improving Reproducibility: Best Practices for Antibodies

In the midst of beeping lab timers, presentations and grant deadlines, it is easy to take for granted the quality of lab reagents.

Sepharose Fast Flow: Purification with Good Resolution and Easy Scale-Up

This page covers the use of Sepharose Fast Flow for purification of proteins.