Table 1.
Real-time PCR primer sequences and optimized concentrations
Gene name | Gene symbol | Primer sequences | Concentrations |
---|---|---|---|
ATP synthase δ subunit | Atp5d | F, 5′ CTCCTCTGTGCAGTTACTAGCTGAA 3′ | 600 nm |
R, 5′ ACTGCGCCTTCTCCAGGTT 3′ | 600 nm | ||
ATP synthase γ polypeptide 1 | Atp5c1 | F, 5′ GAAGGAGTCCACCACCAGTGA 3′ | 150 nm |
R, 5′ CGTTCTTGCTGGCGTTGTC 3′ | 150 nm | ||
Complement component 1 q subcomponent | C1qb | F, 5′ CACCAACGCGAACGAGAACT 3′ | 600 nm |
β polypeptide | R, 5′ GGCCAGGCACCTTGCA 3′ | 600 nm | |
Cyclin D2 | Ccnd2 | F, 5′ GCTCTGTGCGCTACCGACTT 3′ | 300 nm |
R, 5′ CCACGCTTCCAGTTGCAAT 3′ | 150 nm | ||
Cyclin E2 | Ccne2 | F, 5′ TTTTACCTCCATTGAAGTGGTTAAGA 3′ | 600 nm |
R, 5′ GCACCATCCAGTCTACACATTCC 3′ | 600 nm | ||
Cyclin I | Ccni | F, 5′ CACACGGCTACACCATTGGA 3′ | 300 nm |
R, 5′ AAAAGTAACTGAGGCCTAGCTGACA 3′ | 600 nm | ||
Dynein cytoplasmic light chain 1 | Dnclc1 | F, 5′ GGCCCATATCAAGAAGGAGTTTG 3′ | 300 nm |
R, 5′ CATGTGTCACATAACTACCGAAGTTTC 3′ | 300 nm | ||
Kinesin 1b | Kif1b | F, 5′ GGAAGGTCTGCTGAATGCTTTT 3′ | 300 nm |
R, 5′ AATAATCTCTCGGCTGACGATCTC 3′ | 150 nm | ||
Kinesin 5b | Kif5b | F, 5′ GAGTGCAATGTTGATGTCCTAGAAG 3′ | 300 nm |
R, 5′ ACAGTGAAGACACGAAGGACACA 3′ | 300 nm | ||
Malate dehydrogenase 1 | Mdh1 | F, 5′ CCATCGCAGACCACATCAGA 3′ | 150 nm |
R, 5′ AACACCCATCGACACGAACTC 3′ | 150 nm | ||
Necdin | Ndn | F, 5′ GCAGTGTCTCTGAGGACTAAAAAGGT 3′ | 300 nm |
R, 5′ GACTCAACCCCACCCTTACACA 3′ | 600 nm | ||
Plexin domain containing 1 | Plxdc1 | F, 5′ CCACAGAAGATGACACCAAGTTG 3′ | 300 nm |
R, 5′ ACCCTTGGACTTCGGAGATGA 3′ | 300 nm | ||
Glyceraldehyde-3-phosphate dehydrogenase | Gapdh | F, 5′ GCTACACTGAGGACCAGGTTGTCT 3′ | 300 nm |
R, 5′ AGCCCCGGCATCGAA 3′ | 300 nm |
F, Forward; R, reverse.