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. 2016 May 6;7(3):205–209. doi: 10.1016/j.phrp.2016.04.004

Table 1.

Primers for reverse transcription-polymerase chain reaction used in the study.

Virus Primer Sequence (5′→3′) Position Size (bp)
BEBOV Forward GCAGAAATATGCTGAATCTCGTGAAC 1062 418
Reverse ATCATCCTCGTCCTCAAGGTCAAAA 1479
REBOV Forward CCAACAATATGCTGAGTCCAGAGAA 1062 419
Reverse CATCCTCATGATCGTCAAGATCG 1480
SEBOV Forward ACACGTGAGTTGGACAACCTT 1078 402
Reverse GTCATCGTCGTCGTCCAAATTGAA 1479
TEBOV Forward AATCTCGCGAGCTTGACCAT 1076 404
Reverse CTCGTCACCATCTTCAAGGTCAAA 1479
ZEBOV Forward CGAACTTGACCATCTTGGACTTG 1083 399
Reverse TCCTCGTCGTCCTCGTCTAGAT 1481
MMARV Forward AGGCGACATGAACATCAGGAAATT 1012 398
Reverse TCGTCCTCATTCAGCAGTGCAAAT 1409
RMARV Forward GCGACATGAACACCAGGAAATTC 1014 412
Reverse ATTTTCAAGAGTATCCTCGTCTTCG 1425

BEBOV = Bundibugyo EBOV; bp = base pair; MARV = Marburg virus; MMARV = MARV-Musoke; REBOV = Reston EBOV; RMARV = Ravn virus; SEBOV = Sudan EBOV; TEBOV = Taï Forest EBOV; ZEBOV = Zaire EBOV.