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Table 2 The primers and gene ID, used for qRT-PCR analysis

From: Analysis of differentially expressed genes in two immunologically distinct strains of Eimeria maxima using suppression subtractive hybridization and dot-blot hybridization

 Gene ID

Forward primer (5′-3′)

Reverse primer (5′-3′)

  18 s rRNA

CTAACGCAAGGAAGTTTGAGGCA

TACAAGAGGCAGGGACGTAATCG

  S36

CAACTCTGAAGCCTGAACTGGC

CTGTCATTGTGGACCTTGCAAC

  S251

GTCCAACCGCAATAACATCG

CACTTTCGCAACGGAACTCA

  S229

ATTCAGGCACCCGCACTAT

TACGGCGGAACTATCACCAAT

  S231

TAGGTTGCTGCTAACCATACAGG

CACACGGCATCCACTTCAG

  N140

CTTGCACCGCACAGCATAATGT

TCGTCCTGAGTGGAGGCTTTCT

  N214

ATAGTCGGGAATCCAACAACTG

GCCAACCCTACTGCTTGCTG

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Parasites & Vectors

ISSN: 1756-3305

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