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. 2009 Oct 9;10(6):815–828. doi: 10.1111/j.1364-3703.2009.00585.x

Table 5.

Sequences of primers used in this study. The 5′ ends of RanBPM clones 22E10 and 33H17 are identical and the 22E10 F primers were therefore used for both of these genes.

Primer Sequence (5′–3′) Gene and use
J21C1F CAAAGACACAGGCAGCGTAA J21C1 (SPRYSEC homologue) in situ hybridization
J21C1R TCCGTTCAATCCAAAGTTCG J21C1 (SPRYSEC homologue) in situ hybridization
GpUBIF AAGACACTGACCGGCAAAAC Ubiquitin‐like protein in situ hybridization
GpUBIR CGAAGGACCAGGTGAAGAGT Ubiquitin‐like protein in situ hybridization
Up2‐5F GGACAAGGAGCACAAAGAGC Up‐regulated Contig2–5 in situ hybridization
Up2‐5F ATGGACGTCTCCGAGTTCAC Up‐regulated Contig2–5 in situ hybridization
ABAF CAAAGAGGCTGCGAGTCCAT ABA1 homologue in situ hybridization
ABAR TTCAGCGTGCCCCGCCGATC ABA1 homologue in situ hybridization
Rbp1trvgw5F GGGGACAAGTTTGTACAAAAAAGCAGGCTAAATGGCATCGCCAAAACCAAAC SPRYSEC homologue rbp‐1 cloning into TRV2.2b.GW‐GFP
Rbp1trvgw5R GGGGACCACTTTGTACAAGAAAGCTGGGTTTAAATTCTCGTTTTTCAGTTTCTC SPRYSEC homologue rbp‐1 cloning into TRV2.2b.GW‐GFP
Rbp1trvgw3F GGGGACAAGTTTGTACAAAAAAGCAGGCTAGCATCGCCAAAACCAAAC SPRYSEC homologue rbp‐1 cloning into TRV2.2b.GFP‐GW
Rbp1trvgw3R GGGGACCACTTTGTACAAGAAAGCTGGGTTTATAAATTCTCGTTTTTCAGTTTCTC SPRYSEC homologue rbp‐1 cloning into TRV2.2b.GFP‐GW
13G11trvgw5F GGGGACAAGTTTGTACAAAAAAGCAGGCTAAATGACACCAAAAACACCAAACACCAAACTC SPRYSEC homologue 13G11 cloning into TRV2.2b.GW‐GFP
13G11trvgw5R GGGGACCACTTTGTACAAGAAAGCTGGGTTAATCAAGTCGTTAATGTTGAA SPRYSEC homologue 13G11 cloning into TRV2.2b.GW‐GFP
13G11trvgw3F GGGGACAAGTTTGTACAAAAAAGCAGGCTAACACCAAAAACACCAAACACCAAACTC SPRYSEC homologue 13G11 cloning into TRV2.2b.GFP‐GW
13G11trvgw3R GGGGACCACTTTGTACAAGAAAGCTGGGTTTAAATCAAGTCGTTAATGTTGAA SPRYSEC homologue 13G11 cloning into TRV2.2b.GFP‐GW
22E10trvgw5F GGGGACAAGTTTGTACAAAAAAGCAGGCTAAATGTCGCCAAAACCGTCAAACACC SPRYSEC homologue 22E10 cloning into TRV2.2b.GW‐GFP
22E10trvgw5R GGGGACCACTTTGTACAAGAAAGCTGGGTTCAAAGATATCGAAATCCCGG SPRYSEC homologue 22E10 cloning into TRV2.2b.GW‐GFP
22E10trvgw3F GGGGACAAGTTTGTACAAAAAAGCAGGCTATCGCCAAAACCGTCAAACACC SPRYSEC homologue 22E10 cloning into TRV2.2b.GFP‐GW
22E10trvgw3R GGGGACCACTTTGTACAAGAAAGCTGGGTTTACAAAGATATCGAAATCCCGG SPRYSEC homologue 22E10 cloning into TRV2.2b.GFP‐GW
24D4trvgw5F GGGGACAAGTTTGTACAAAAAAGCAGGCTAAATGGGGAACGAACAAAATGCATATG SPRYSEC homologue 24D4 cloning into TRV2.2b.GW‐GFP
24D4trvgw5R GGGGACCACTTTGTACAAGAAAGCTGGGTTAATGCCATCGGCAAAGTTG SPRYSEC homologue 24D4 cloning into TRV2.2b.GW‐GFP
24D4trvgw3F GGGGACAAGTTTGTACAAAAAAGCAGGCTAGGGAATGAACAAAATGCATATG SPRYSEC homologue 24D4 cloning into TRV2.2b.GFP‐GW
24D4trvgw3R GGGGACCACTTTGTACAAGAAAGCTGGGTTTAAATGCCATCGGCAAAGTTG SPRYSEC homologue 24D4 cloning into TRV2.2b.GFP‐GW
33h17gw5R GGGGACCACTTTGTACAAGAAAGCTGGGTTATCTTTTGGCAATAAATTCTTG SPRYSEC homologue 33H17 cloning into TRV2.2b.GW‐GFP
33h17gw3R GGGGACCACTTTGTACAAGAAAGCTGGGTTTAATCTTTTGGCAATAAATTCTTG SPRYSEC homologue 33H17 cloning into TRV2.2b.GFP‐GW