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qRT-PCR was carried out in triplicate with isoform specific primer-pairs sequences of which are given in Table 2. The nucleotide sequences of the Primer-pair for amplification of 16 S rRNA is presented in Table 2. cDNA for TPM4-2 were made with Exon (A(−) oligonucleotide (Table 2) whereas oligo dT was used for TPM4-1α cDNA.
TOP: TPM4-1α; Bottom: TPM4-2α
