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. 2016 Sep 23;6:33885. doi: 10.1038/srep33885

Table 1. Primers and PCR conditions.

Primer Name Sequence (5′–3′) Tm (°C) No. of cycle
psbA qPCR forward TGCCATTATTCCTACTTCTGCA 60 30
psbA qPCR reverse AGCACTAAAAAGGGAGCCG 60 30
psaA qPCR forward GCAGGGCTACTAGGACTTGG 60 30
psaA qPCR reverse GGCCTGTAAATGGACCTTTATG 60 30
petA qPCR forward CAGCAGAATTATGAAAATCCACG 60 30
petA qPCR reverse TATTAGTAGCAGGGTCTGGAGCA 60 30
ATFD2 qPCR forward ACTTCATTCATCCGTCGTTCC 60 30
ATFD2 qPCR reverse AAGAACCAGCACGGCAAG 60 30
LHCB1.1 qPCR forward CCGTGTGACAATGAGGAAGA 60 30
LHCB1.1 qPCR reverse CAAACTGCCTCTCCAAACTTG 60 30
ATBCA3 qPCR forward CGAGTTCATAGAAAACTGGATCC 56 35
ATBCA3 qPCR reverse AGGCAGGGGTAGTCTTGAAGT 56 35
APX1 qPCR forward GGACGATGCCACAAGGATA 58 35
APX1 qPCR reverse GTATTTCTCGACCAAAGGACG 58 35
GST qPCR forward TCTATAAAACACCATACCTTCCTTCA 58 35
GST qPCR reverse CGAAAAGCGTCAAATCACC 58 35
PP2AAC qPCR forward GCGGTTGTGGAGAACATGATACG * *
PP2AAC qPCR reverse GAACCAAACACAATTCGTTGCTG * *

*The annealing temperature and PCR cycles of PP2AAC ‘housekeeping’ gene is dependent on the PCR condition of the genes being studied.