I've odered primers from IDT.
In the IDT FAQ it is suggested to add 10 microliters of water per 1 nanomole to obtain 100 µM concentration. But in my calculations the final concentration is 1µM/µL. Am I wrong somwhere? How can you possibly get micromoles (10-6) from nanomoles (10-9) by dilution?
This is the link to the IDT manual http://www.idtdna.co...-concentration-
Thank for help!
Primer concentration - stupid question
Started by Angrysh, Jun 04 2013 04:51 PM
3 replies to this topic
#1
Posted 04 June 2013 - 04:51 PM
#2
Posted 04 June 2013 - 06:10 PM
You are confusing moles with molar. 1 molar (1 M) is 1 mole per liter. The IDT instructions are 1 nanomole per 10 microliters, which is 10**-9 moles/ 10**-5 liters, or 10**-4 molar, or 100 uM.
#3
Posted 04 June 2013 - 08:03 PM
Thank you!
Now it is clear. So molar concentration is always per liter?
Now it is clear. So molar concentration is always per liter?
#4
Posted 05 June 2013 - 01:36 AM
Yes, Molar concentrations are always per litre -it's the SI unit. It is a bit of an unfortunate thing that biologists (including myself) have gotten into using the "M" symbol for mol/l as it is quite confusing until you know the convention.













