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Lab methods, plainly

The workhorse methods of a molecular lab

A handful of techniques account for most of the work in a molecular biology lab. None of them is exotic, and each has a short list of failure modes that explain most bad results.

Extraction comes first

Almost every downstream method starts with getting nucleic acid or protein out of a sample and away from whatever would interfere. Poor extraction shows up later as weak amplification, smeared gels or inconsistent replicates — and gets blamed on the later step.


Amplify, separate, check

A typical workflow amplifies a target, separates the products by size, and confirms that what came out is what was expected. Each step can hide a problem from the one before it.


Contamination is the constant enemy

Sensitive methods detect tiny amounts of material, including material that should not be there. Physical separation of pre- and post-amplification work and consistent negative controls do more for reliability than any single reagent choice.

More pages

  1. PCR and RT-PCR: how amplification works and fails
  2. Gel electrophoresis: separating DNA and proteins by size
  3. Filtration in the lab: membranes, pore sizes and uses
  4. Why this site exists