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Anthers from dried flower buds were treated by standard acetolysis method (Erdtman 1960).
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The caspase 3 activity in each sample solution was calculated by standard curve method.
DNA was extracted by standard salt method.
The results of the method were validated by standard method.
Cured strains were reevaluated for their MIC for ceftriaxone and meropenem by standard microbroth dilution method.
Cleavage by thrombin (Sigma) was performed by standard method.
Total protein concentration was determined by standard method.
Bacterial and fungal organisms were identified by standard microbiological methods.
Genotypic analyses were performed by standard PCR methods.
Chemical data were determined in triplicates by standard oceanographic methods.
All constructs were verified by standard sequencing methods.
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