Reverse Transcriptase-Polymerase Chain Reaction Validation of 25 “Orphan” Genes from Escherichia coli K-12 MG1655

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 2.Figure 2.Figure 2.
Figure 2.

Control experiments required to validate each of the results in Table1. (a, b) Series of experiments corresponding to Figure 1, in absence of reverse transcriptase (RT) (no band expected). (c) Other RT-polymerase chain reaction (PCR) and PCR reaction controls. (M) Molecular Weight Marker VI (Boehringer Mannheim). Validation of RT reactions using kanamycin mRNA (kit control): water instead of matrix with kanamycin primers (lanes 1 and 5) (no band expected), with kanamycin mRNA (lanes 2 and 6) (band expected). Validation of PCR reaction using MG1655 E. coli genomic DNA: water instead of matrix with rpoD primers (lane3), or rpoS primers (lane 7) (no band expected), genomic DNA with rpoD primers (lane 4), or rpoS primers (lane 8) (band expected).

This Article

  1. Genome Res. 10: 959-966

Preprint Server