Reconstituting primers-PDF

Procedure

Invitrogen recommends the following reconstitution procedure –

1. Centrifuge the tube for a few seconds to get all the DNA to the bottom of the tube.
2. To make a 25 μM stock, add YμL of sterile H₂O to X nmoles of dry primer stock. (See equations below).
3. Allow to sit for 2 mins, then vortex for 15 secs.

Short version

[math]\displaystyle{ Y\ \mu L\ =\ 40\ *\ X\ nmoles\ primer }[/math]

The number of nmoles of material in the tube (X) should be listed on the pages accompanying your primer order.

Long version

[math]\displaystyle{ Y\ \mu L\ =\ \frac{1 L}{25\ \mu moles}*X\ nmoles\ primer\ =\ \frac{1*10^6\ \mu L}{25000\ nmoles}*X\ nmoles\ primer\ =\ 40\ *\ X\ nmoles\ primer }[/math]

Notes

See Reconstituting primers for a lot of useful information including why you should use TE buffer rather than water for reconstituting primers.