Figures & data
Figure 2. PCR amplification products of NBS RGAs in mango. M: DNA Marker V; Lane 1: blank control; Lane 2: control using water as a template; Lane 3: PCR products of NBS genes amplified with forward and reverse primers for mango.
![Figure 2. PCR amplification products of NBS RGAs in mango. M: DNA Marker V; Lane 1: blank control; Lane 2: control using water as a template; Lane 3: PCR products of NBS genes amplified with forward and reverse primers for mango.](/cms/asset/92b611ac-673d-4a7f-b938-1274a79af996/tbeq_a_931706_f0002_b.gif)
Table 1 Variation sites of 16 RGAs sequences in mango.
Figure 4. Polymorphism characteristic of NBS–LRR analogues isolated from mango (pp-01–16). The vertical axis represents the nucleotide diversity (Pi), and the horizontal axis represents the nucleotide position (bp), the curved line represents the change of Pi in different nucleotide positions.
![Figure 4. Polymorphism characteristic of NBS–LRR analogues isolated from mango (pp-01–16). The vertical axis represents the nucleotide diversity (Pi), and the horizontal axis represents the nucleotide position (bp), the curved line represents the change of Pi in different nucleotide positions.](/cms/asset/a62f3ea7-54db-4d07-a983-d2b8294fc1f7/tbeq_a_931706_f0004_oc.jpg)
Table 2 Results from the BL2SEQ algorithm showing the extent of identity between the RGAs isolated in the present study.