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. 2018 Mar 23;10(4):144. doi: 10.3390/v10040144

Table 1.

Primers used in this study to complete the genome sequence of the PM14 isolate.

Primer Name Sequence (5′-3′) Genome Coordinates Amplicon Size (nt)
Capillo-mume-5Race2 # CCTTGCATGGTTGTTGTTGAAGTCCTCCC 251–223 252
Capillo-mume-F1 AACAACAACCATGCAAGGTTTGAG 234–257 503
Capillo-mume-R1 GCTAGAACACACTTAGGCCGCAA 736–714
Capillo-mume-F2 GGAATGTTGATACATACAGACA 1629–1650 742
Capillo-mume-R2 CGTCTGAGCCTAATCCATACAC 2370–2349
Capillo-mume-F3 TGGATTTATTGAACTTCTCATAC 2831–2853 406
Capillo-mume-R3 CGTCACAATCACACCAAATCTG 3236–3215
Capillo-mume-F6 GATGTACGAGGATTCAGTGG 4034–4053 451
Capillo-mume-R6 AATGAGGGAGTTAGAAACACC 4484–4464
Capillo-mume-R7 ~ ACCAACTGTTATGACAGATTC 5117–5097 1084
LD-PolyT @ CACTGGCGGCCGCTCGAGCATGTAC(T)25NN
Capillo-mume-LD GAGCACCATTGGAGGGTGTGT 7462–7482 183
LD-Prime CACTGGCGGCCGCTCGAGCATGTAC

# This reverse primer was used in conjunction with the universal primer provided by the 5’ RACE kit (Takara Bio Europe/Clontech, Saint-Germain-en-Laye, France); ~ This reverse primer was used in conjunction with the Capillo-mume-F6 primer; @ This primer was used for the complementary DNA synthesis prior amplification with the primer pair Capillo-mume-LD and LD-Prime.