Prepare in a sterile tube:

 

template RNA:

 

total RNA  0.1-5μg

 

or poly(A)+ mRNA  10ng-0.5μg,

 

or specific RNA  0.01pg-0.5μg

 

primer:

 

oligo(dT)18   0.5μg

 

or random hexamer 0.2μg,

 

or sequence-specific 15-20pmol,

 

deionized water (nuclease free) up to 11μl.

 

Incubate the mix at 70℃for 5 minutes and chill on ice.

 

Add the following in the order indicated:

 

5X reaction buffer 4μl,

 

10mM 4 dNTP mix 2μl (1.0mM - final concentration),

 

ribonuclease inhibitor 20u,

 

deionized water (nuclease free) to 19μl.

 

Incubate at 37℃for 5 minutes. If random primer is used, incubate at 25℃for 5 minutes.

 

Add 40 units of M-MuLV Reverse Transcriptase . Incubate the reaction mixture, containing oligo(dT)18 or sequence-specific primer at 37℃for 60 minutes. If using random hexamer primer, incubate at 25℃for 10 minutes and then at 37℃for 60 minutes.

 

Stop the reaction by heating at 70℃for 10 minutes. Chill on ice.

 

Note

 

The synthesized cDNA can be amplified by the PCR (see Protocols for PCR using Taq and Pfu DNA Polymerases) without intermediate phenol/chloroform extraction or ethanol precipitation.

 

Reference

 

Gerard, G.F. and D'Alessio, I.M., Methods in Molecular Biology, 16, Humana Press, Totowa, N.J., 73-93, 1993.

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