To monitor the mutations effects about relationships with TL-mRNAs, wt and mutant protein were immunoprecipitated as well as the associated RNAs isolated through the immune complexes were identified simply by quantitative change transcription-PCR with particular primers for TL, fiber, and cellular GAPDH mRNAs (Fig

To monitor the mutations effects about relationships with TL-mRNAs, wt and mutant protein were immunoprecipitated as well as the associated

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