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Figure 1 | Malaria Journal

Figure 1

From: Development of an allele-specific, loop-mediated, isothermal amplification method (AS-LAMP) to detect the L1014F kdr-w mutation in Anopheles gambiae s. l.

Figure 1

DNA sequence of part of the voltage-dependent sodium channel gene surrounding the kdr mutation, and the position of the primers designed for AS-LAMP. Partial kdr gene sequence and location of primers, FIP (F1c-F2), BIP (B1c-B2), F3, and B3. The nucleotides in red are the regions of the PCR primers used for the PCR product inserted into the plasmid. The mutated nucleotide in kdr-w is shown in bold blue type, A for the wild type and T for the West African-type (kdr-w).

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