Fig. 3- Photos (Gel electrophoresis) to amplify the DNA by PCR
technique
Sequence Alignment
Sequence alignment was performed using ClustalX version 1.81
[40] with gap opening penalty 10 and gap extension penality 3.0.
Sequence alignments was subsequently adjusted manually using
BioEdit [41]. Insertion-deletions (Indels) were scored as single char-
acters when we had confidence in positional homology. Gaps were
treated as missing
data in phylogenetic analysis.
Sequence Retrieved from GenBank
ITS sequences of nrDNA of 19 species of Limonium and Outgroup
[Table-4] were retrieved from GenBank database of National Center
for Biotechnology Information (www.ncbi.nlm.nih.gov). The generic
classification of the Limonium has been present in the [Table-5].
The boundaries between the ITS1, 5.8S, and ITS2 gene for the
data set (both the sequence generated for the present study and
the sequences retrieved from the GenBank) were determined ac-
cording to span mentioned in features of the nrDNA ITS sequences
available in GenBank. ITS2 sequences were extracted from the
complete set of the ITS sequence and used in the further analysis.
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