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. Author manuscript; available in PMC: 2009 Jul 6.
Published in final edited form as: Mol Biochem Parasitol. 2007 Sep 15;156(2):246–254. doi: 10.1016/j.molbiopara.2007.09.001

Fig. 6.

Fig. 6

TbCgm1 is recruited to the SL RNA genes in vivo. Chromatin immunoprecipitations were performed with antibodies directed against the BB2 epitope tag present on TbCgm1 (lanes 3 and 6) or TbCe1 (lanes 9 and 12), or with no antibodies as a control (lanes 2, 5, 8 and 11). PCR amplification of the immunoprecipitates was done with primers upstream of the SL promoter (nt −608 to −530) or within the promoter (nt −56 to +82). Numbering is with respect to the SL RNA transcription start site. An aliquot of the total input is also shown (lanes 1, 4, 7 and 10).

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