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. 2008 Jun 25;9:301. doi: 10.1186/1471-2164-9-301

Table 2.

Characteristics of the RT-qPCR analysis of differentially expressed genes of Apis mellifera

Product name Honey bee ID Forward primer sequences Reverse primer sequence Amplicon size (bp) Amplification efficiencya(Rb)
Krh1 GB14867 ACTCATCAGTTGTTGGTTCTCCTC TCGTTTGGCTCTTCAGTCTTGTG 118 2.11 (0.99)
non determined GB18554 TCACACCGATATTCTCATCAAAGG CTTGTCATTCTTGTTCTCCGATTG 112 1.94 (0.98)
Hr78 GB18358 TGACGAAGTTTAGTTGCTGCTATG TGTTGTTCCCTATGATCTCTGTCC 107 1.98 (0.99)
Alh GB17400 ACTTGTGGTAATGCTGGCTGAC AACGAACGAAGGAAAGGAATAACG 129 2.08 (0.96)
baz GB10346 ACCAGGAACAAGCGAGTCAGAAG ACCAGGAACAAGCGAGTCAGAAG 112 2.02 (0.99)

Honey bee IDs refer to the cDNAs selected from the EST microarray experiment (see text).

Krh1 is the housekeeping gene. Forward and reverse primer sequences and the PCR product length are indicated.

aAmplification efficiencies were calculated from the slope of standard curves as E = 10 [-1/slope] – 1.100% efficiency corresponds to an amplification efficiency of 1; bRegression coefficient of linear standard curve.