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. 2011 Nov 25;2:234. doi: 10.3389/fmicb.2011.00234

Table 1.

Genes and primers used to amplify targets for plasmid standards (PCR) and measure transcript abundance (qRT-PCR) in T. pseudonana.

Target gene/protein ID/Accession number Reaction type Primer direction Primer sequence (5′–3′)
Fe reductase (chr 3)/3129/XP_002288167 PCR Forward TCAACGTTTTCTTCTGGAGTCA
Reverse ATTCTCCGCAGCACATTTTT
qRT-PCR Forward TCGTGGGCATGTATCTTCATG
Reverse GCCTCCGTAGCAGACTATTGATG
Probea TCCTGGTGCTCGTCCCTTCATCCTC
Fe reductase (chr 19)/11375/XP_002297175 PCR Forward TGGTAGCACATCCTTTCACGGTCA
Reverse ATGGAGAGAAACGTTGCAAACGGC
qRT-PCR Forwardc GCCGTACTTGACAATGCTGA
Reversec ACCAGTGAAATGCACGATGA
Probea AAGTCTCCTCTCACGAAATCAGTGGAGC
Multicopper oxidase/5574/XP_002290775 PCR Forward TGGGAGTTTGGTACATGCAA
Reverse GCGACACATCCAGAAGGTTT
qRT-PCR Forward CGGTGGTGGCTGCTGATT
Reverse TCTCCGACGTGTACCACAACTT
Probea AGTTGAAGCGTTTACTGTAGAC
Cu transporter (chr 7)/35496/XP_002295670 PCR Forward GTCGTTTGGGCATTGCTACT
Reverse CAATCACCTTCTGACGAGCA
qRT-PCR Forward GCCTGCCCTTGTGCATTG
Reverse TGCTCCTATTCCGGTTCCAA
Probea ATTGGCCACGCCTACTGCCGTCAT
Cu transporter (chr 16)/264357/XP_002296688 PCR Forward CCAACGGATGGAGTGCTAAT
Reverse AGGGACACGCCACTACAATC
qRT-PCR Forward TCCAAGCTCAGGCTGATCGT
Reverse TGTAGCGGCAGCAACTAGCA
Probea TTGCATCCATCTTTGCTCCGATCGTC
Flavodoxin/28635/XP_002291468 PCR Forward AAGTGGGCGTCTTCTTCGGTACTT
Reverse TCTCCACGCTGAGCCTTTGATTCT
qRT-PCR Forward TGCGAAGTATGATGCTTTAGTGGTA
Reverse CCAGCCCGTTCCACTACGT
Probea CCAACATGGAACACTGGTGCTGACACTG
Ferredoxin/YP_874492 PCR Forward GTCTGATCTTCCAAAGATTCAAATCGGG
Reverse CCAGCACCCATTTGATCATCATC
qRT-PCR Forward AGATGCAGCAGAAGAAGCAGGA
Reverse ACCATCTGATACTTTACCAGCACA
Probea CTTGTCGTGCTGGTGCTTGTTCTACA
Actin/25772/XP_002294917 PCR Forward ACGTGACCTCACGGACTACC
Reverse CAAAGCCGTAATCTCCTTCG
qRT-PCR Forward GTGGACTTTGAGGAGGAGATGAA
Reverse CAGGGAGCTCGAAGGACTTCT
Probeb GGCTGCGGAGTCGTCGGCTCT

aProbe labeled with 5′-FAM and 3′-BHQ.

bProbe labeled with 5′-HEX and 3′-BHQ.

cPrimer pair used in Kustka et al. (2007).