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From:
Published online 2009 April 8. doi: 10.1186/1471-2164-10-152

Figure 1

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Antisera against TBP and SNAP50 preferentially precipitate tRNA/snRNA sequences. L. major chromatin was immunoprecipitated using antisera against TBP (top panel) or SNAP50 (middle panel) and PCR amplification carried out using primers specific for the U2/tRNAAla locus on chr31, which is bound by both TBP and SNAP50 in L. tarentolae [24] and the LmjF01.0530 gene on chr1 as a control. The numbers at top represent PCR cycles. The input control in the bottom panel represents amplification of chromatin without immunoprecipitation.

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