Method Article
June 10th, 2011
A correction to the step 2 of Part 1 for article Visualizing RNA Localization in Xenopus Oocytes.
A correction was made to Visualizing RNA Localization in Xenopus Oocytes. There was an error in step 2 of part 1. Some characters in the reagents table had the incorrect symbols. This was corrected to:
a. 10X Tx buffer (see M&M) | 2 μl |
b. 20X cap/NTP mix (see M&M) | 1 μl |
c. 1 mM Alexa Fluor 546-14-UTP (Invitrogen) | 1 μl |
d. UTP, [α-32P](1 μCi/μl) (Perkin Elmer) | 1 μl |
e. DEPC-H2O | 11 μl |
f. 0.2 M DTT | 1 μl |
g. RNasin (Promega) | 1 μl |
h. linear template DNA | 1 μl |
i. RNA Polymerase (Promega) | 1 μl |
instead of:
a. 10' Tx buffer (see M&M) | 2 μl |
20' cap/NTP mix (see M&M) | 1 μl |
1 mM Alexa Fluor 546-14-UTP (Invitrogen) | 1 μl |
UTP, [α-32P](1 μCi/μl) (Perkin Elmer) | 1 μl |
a. DEPC-H2O | 11 μl |
b. 0.2 M DTT | 1 μl |
c. RNasin (Promega) | 1 μl |
d. linear template DNA | 1 μl |
e. RNA Polymerase (Promega) | 1 μl |
No conflicts of interest declared.
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