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Table 1 Summary of aptamers reported previously to bind to PLDHs that were used in this study

From: A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices

Aptamer

Reported sequence, sourced for this study (5′-3′)

Binding buffer used

Reference

LDHp1

GCCTGTTGTGAGCCTCCTAACCAGGAAGCGACCTACTAAAGTGATATTAT AGATTCACGGGAGCGTGGTGCATGCTTATTCTTGTCTCCC

2 mM HEPES,

0.2 mM MgCl2,

0.2 mM CaCl2,

0.2 mM KCl,

15 mM NaCl,

pH 7.4

[12]

LDHp11

GCCTGTTGTGAGCCTCCTAACCTACTGTTGATATGAGTGATAGGGCGGCG CGCTTATCTAGTGTATTGTGCATGCTTATTCTTGTCTCCC

rLDH4

GCCTGTTGTGAGCCTCCTAACCAGCTCGTAGAAAAAAAAAGATATTGCTTCAATTATCTCCTCGCGTTCAATTAACCCAGCATGCTTATTCTTGTCTCCC

rLDH7

GCCTGTTGTGAGCCTCCTAACCCAGAATAGGGACTGCTCGGGATTGCGGA TGAGTCTGGGTGGGACATGGCATGCTTATTCTTGTCTCCC

rLDH15

GCCTGTTGTGAGCCTCCTAACTTTAAAGTTGCTATTTAACCAAAAAAAAAAAAATAAAAAAGTCGAGCCGGCCCATGCTTATTCTTGTCTCCC

pL1

CACCTAATACGACTCACTATAGCGGATCCGACTCACGTACAGCAAGGTTC GATTGGATTGTGCCGGAAGTGCTGGCTCGAACAAGCTTGC

20 mM Tris–HCl, 50 mM NaCl,

5 mM KCl, 5 mM MgCl2,

300 mM imidazole, pH 8.0

[10]

2008s

CGTACGGTCGACGCTAGCCTGGGCGGTAGAACCATAGTGACCCAGCCGTC TACCACGTGGAGCTCGGATCC

10 mM Na2HPO4, 1.8 mM KH2HPO4, 2.7 mM KCl, 137 mM NaCl, pH 7.4

[11]

  1. Bolded sections of the reported sequences refer to primer-binding sites used during SELEX, while unbolded sequences refer to the variable regions.