Question #81879

You order a PCR primer from Eurofins Genomics. They deliver a tube with 35 nmoles of DNA
in it. How much TE buffer do you need to turn it into a 100 µM freezer stock? Which pipettor
should you use? To what should it be set?

Expert's answer

Question #81879, Biology, Genetics

Question:

You order a PCR primer from Eurofins Genomics. They deliver a tube with 35 nmoles of DNA in it. How much TE buffer do you need to turn it into a 100 μM freezer stock? Which pipettor should you use? To what should it be set?

Solution:

Molar concentration can be calculated from the equation:


C=vVC = \frac {v}{V}


where C – molar concentration, v – number of moles, V – volume.

From the equation:


V=vCV = \frac {v}{C}


As the required molar concentration is C = 100 μM, v = 35 nmol, then:


V=vC=35 nmol100μM=35×109 mol100×106M=0.35×103L=350μLV = \frac {v}{C} = \frac {35 \text{ nmol}}{100 \mu M} = \frac {35 \times 10^{-9} \text{ mol}}{100 \times 10^{-6} M} = 0.35 \times 10^{-3} L = 350 \mu L

Answer:

To make the required freezer stock, 350 μL should be added into a tube using a pipettor of the volume 1 mL set to 350 μL.


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