Skip to main content

Table 5 Sequence of gene-specific primers used for real-time PCR analysis.

From: Differential transcript expression between the microfilariae of the filarial nematodes, Brugia malayi and B. pahangi

Pub locus

Forward primer

Reverse primer

Bm1_49585

GACCGAAACAAGAAAGGAAGCCGA

ACTTTCATCATCATTATGTCGTCGCG

Bm1_11050

GATGAAACGTTTCATGAGATG

GATAATCCTCCAAAACTACCG

Bm1_02070

AATAATTGGATTTCGAGTGAGAC

TTCATGCATAATTACCAGTTTCG

Bm1_28420

AAGGCTTCGATATGTTTCCATC

CTAACCACTAGTACATATTGTCT

Bm1_42865

AAACATGCAGTTAATGCACGAG

TGCTTGCAATTCATTCCTCACT

Bm1_19100

GCCACAAGGTATGCAACCACA

GTGTCTGCGTGGGTGGTAAC

Bm1_25950a

GCTAACTTCAATGCACTTAGTG

AAATAAGAAACAACGTTTGATACAG

Bm1_01300a

CAATTTTCAGACTCAATCTACTG

AGGTAAGTATTTGTCAACGTTTG

Bm1_44655a

GTACGAAAGCAAGGATTCTGCT

CAGAATACTTTGTAGGTATCATTC

Bm1_50670a

GTATTAGCTCAAGCAATGGAAG

CTAACTACTATCATCACTATTATC

bm.02018ab

AGAATCAAATGTCCAGGAAG

CTGTGAGAGGAAGATAGTC

BMX9555b

TTGATGTAGATGCTTTAACAAGTGCTGCTC

AAGAAATTGTCGACAAAGTCCGCAAG

BMX10185b

CCGCACAACAATCCTCACTTGCT

TGTGTTACTGCTATTAACATCCTCACTGCC

  1. Each primer is written in the 5' to 3' direction.
  2. a Indicates the genes whose probe regions were amplified and sequenced using the primers shown.
  3. b Indicates the probes whose primers were used to determine a suitable endogenous control for real-time PCR analysis.