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. 2011 Nov;77(21):7823–7829. doi: 10.1128/AEM.05822-11

Table 1.

Oligonucleotides used in the study

Oligonucleotide name Sequence (5′ → 3′)a Description
MC840 gtatgcggccgctccacacacagtggaggg Amplification of the 5′ region of uhd1 for deletion construct
MC841 cacggcctgagtggcctgtgagcagttgtacatgg
MC842 gtgggccatctaggcctcgtatagcaacggatgaaattcgtg Amplification of the 3′ region of uhd1 for deletion construct
MC843 cacagcggccgccaagaatcgatgcttgccgg
RB89 gagccatggtaaaaatgacaaaggaagccg Amplification of fhd1 ORF
RB90 gaggcggccgcgcccgcccgacgatagttat
RB125a ccatggccacccagactctatc Amplification of ahd1 ORF
RB125b gcggccgctagccgtctggcccgaatac
RB18 agaggagtgaggcggtttgg Amplification of internal probe for gene fat2 (RT-PCR)
RB19 caagagcccaacgctgaacg
RB27 cctcctgctgctgctgctgc Internal control primers for fhd1
RB28 gccattcgaagtgtacatgg
RB72 ccaacgtcttcttcgacatc Amplification of internal probe for gene ppi (RT-PCR)
RB73 gcgccgtagatcgacttgcc
RB112 gcctcctcgccaccgaggtc Amplification of internal probe for gene ahd1 (RT-PCR)
RB113 ggtgccgatgaggaggccgg
a

Underlined letters indicate introduced restriction sites.