
Products · Life Science
Buffers, substrates and the general biochemicals a laboratory consumes rather than studies. Purity here is necessary but rarely sufficient: the specifications that decide whether a lot is usable — endotoxin, nuclease activity, the pH at your working temperature — are separate tests that a chemical certificate of analysis does not report.
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Specifying it
The compound is usually fixed by the route. These are the things that vary between suppliers and between lots.
A buffer controls pH usefully within roughly one unit either side of its pKa and does very little outside that window. Choosing by familiarity rather than by range is how a system ends up nominally buffered and actually drifting. Match the buffer to the pH the assay runs at, not to what the last protocol happened to use.
Tris has a temperature coefficient near −0.03 pH units per degree, so a buffer adjusted to pH 8.0 at room temperature is closer to 8.6 in a cold room and below 7.7 at 37 °C. If a buffer is prepared at one temperature and used at another, state the temperature at which the pH must hold — otherwise the certificate and the experiment refer to different conditions.
A biochemical can be chemically pure and still carry bacterial endotoxin or residual nuclease activity that ruins a cell assay or degrades RNA. These are tested for and certified separately. If the application is biological, the requirement belongs on the enquiry explicitly — assuming a high chemical purity implies either is a common and expensive mistake.
Many buffer salts and biochemicals take up water rapidly on opening. A hygroscopic solid weighed from a jar that has been open on a bench is not the mass of compound you intended, and molarity calculated from it is out. Buy in unit sizes matched to consumption, and store desiccated where the material calls for it.
Questions