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. 2006 May 9;2006:71753. doi: 10.1155/JBB/2006/71753

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Copyright © 2006 Kert Mätlik et al.

This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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TSS mapped to the L1 ASP region. (a) The position of TSS present in the DBTSS is shown highlighted on the consensus sequence of L1Hs [4] between positions 347 and 601. TSS with single and multiple entries present in the database are represented by yellow and blue highlight, respectively. The letters above the sequence mark the 3′ end of the oligonucleotide primers used in RT-PCR (see Table 1). (b) Southern blot RT-PCR analysis of the L1-MET transcripts. The lanes are marked according to the primers used in the PCR. Multiple bands on each lane represented the different splice variants of the L1-MET transcript, as confirmed by sequence analysis.

TSS mapped to the L1 ASP region. (a) The position of TSS present in the DBTSS is shown highlighted on the consensus sequence of L1Hs [4] between positions 347 and 601. TSS with single and multiple entries present in the database are represented by yellow and blue highlight, respectively. The letters above the sequence mark the 3′ end of the oligonucleotide primers used in RT-PCR (see Table 1). (b) Southern blot RT-PCR analysis of the L1-MET transcripts. The lanes are marked according to the primers used in the PCR. Multiple bands on each lane represented the different splice variants of the L1-MET transcript, as confirmed by sequence analysis.