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. Author manuscript; available in PMC: 2009 Sep 2.
Published in final edited form as: J Biol Chem. 2007 Nov 27;283(5):2586–2594. doi: 10.1074/jbc.M707154200

Table 2. PCR primers used in this study.

Primer Sequence (5′ → 3′) Gene
target
NCBI accession
number
Target sequence
position
Product
length
bp
F1 ATGACCGCTTCTGATACAGTCTAC arz1 NC_003421.2 2,325,172-2,325,196 2479
R1 TTCGCAACGCTGGAAAGTTTGTGT 2,327,651-2,327,627
F2 TTTCAATCTCATTCTCACTTTCTGA nmt/arz1 pREP (23) 1,098-1,122 374
R2 GGGCTCGATACTCTCGTGAATCC NM_001023516.1 325-303
F3 CTCTTGAACTCCTTAGGG arz1 NM_001023516.1 98-115 665
R3 TGCTATTAGAGTCGTCGG 763-746
F4 TCCCTTCTTCAGTCATGCCC zfs1 NM_001022372.1 251-270 460
R4 ACAGAGTTGCGGATGTTTGTC 711-690
F5 TTGTTGACTGAGGCTCCTTTGAAC actin NM_001021513.1 310-333 801
R5 AAACGATACCCAGGTCCGCTCTC 1,111-1,090
F6a ATGAGAATATTGGTACCCTGTTTCAGGGTCCGGTTTATTCTCCTATGTCTCG zfs1 NM_001022372.1 4-13 1212
R6a CTCGATTAACTAGTAGCTAGCTCAAGGAGATTGCTTAATAGTTG 1,193-1,215
a

Underlined bases indicate zfs1 specific primer regions, whereas italic text highlights SspI and SpeI restriction sites for cloning into restriction enzyme-digested expression vector.