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. Author manuscript; available in PMC: 2013 Jul 31.
Published in final edited form as: Infect Genet Evol. 2010 Dec 13;11(2):391–398. doi: 10.1016/j.meegid.2010.11.010

Table 1.

Ligase detection reaction primers for genotyping P. vivax variants (VK210 and VK247).

Variant Primer sequencea FlexMap™ microsphere set id no.b
VK210-TAG 5′ cta caa aca aac aaa cat tat caa GGW GAY AGA GCA GMT GGA CAR CCA GCA 3′ 28
VK210 conserved 5′-/5Phos/GGA AAT GGT GCA GGT GGA CAG GCA GCA/3Bio/−3′
VK247-TAG 5′ cta act aac aat aat cta act aac GCA AAT GGR GCN GGY AAT CAA CCA GGA 3′ 80
VK247 conserved 5′-/5Phos/GCA AAT GGT GCA GGT GGA CAG GCA GCA/3Bio/−3′

W= A or T; Y=T or C; M=A or C; R=G or A, N=A, T, C or G.

a

Primers were designed using pvcsp sequence for both subtypes: VK210 (GenBank accession number M11926), VK247 (GenBank accession number M28745). Lowercase nucleotides represent the TAG sequence specific to the FlexMap™ microsphere and are added to the 5′ end of each variant-specfic LDR primer.

b

ID, identification. One hundred unique Luminex microsphere sets are synthesized to exhibit unique fluorescence. Each microsphere set is coupled to different anti-TAG sequences. Anti-TAG sequences are complementary to allele-specific TAG sequences.