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. 2019 May 28;7(10):1582–1587. doi: 10.3889/oamjms.2019.285

Table 1.

The sequences of primers used for AS-LAMP method for the detection of IVSII-I G>A method

Set1: BIP-Wild = B1C (5-3) + B2 (5-3) GTGAGTCTATGGGACGCTTGATTATCCCCTTCCTATGACATGA
Set1: BIP-Mutated = B1C M (5-3) + B2 (5-3) ATGAGTCTATGGGACGCTTGATTATCCCCTTCCTATGACATGA
Set 2: BIP-Wild = B1C (5-3) + B2 (5-3) GTTGAGTCTATGGGACGCTTGATTATCCCCTTCCTATGACATGA
Set2: BIP-Mutated = B1C M (5-3) + B2 (5-3) ATTGAGTCTATGGGACGCTTGATTATCCCCTTCCTATGACATGA
Set3: BIP-Wild = B1C (5-3) + B2 (5-3) GTCAGTCTATGGGACGCTTGATTATCCCCTTCCTATGACATGA
Set3: BIP-Mutated = B1C M (5-3) + B2 (5-3) ATCAGTCTATGGGACGCTTGATTATCCCCTTCCTATGACATGA
FIP= F1C (5-3) + F2 (5-3) CCTGAAGTTCTCAGGATCCACGCCTTTGCCACACTGAGTG
F3 TCACCTGGACAACCTCAA
B3 5’CCATTCTAAACTGTACCCTG3’

Set1: primer designed by http://primerexplorer.jp/lampv5e/index.html, Set2: In this sets of primers 1 nucleotide was inserted at the 5’ end of BIP primers, Set3: The sequence of primers in which one nucleotide at the 5’ end of BIP primer was changed