Qualitative analysis detects Cry1Ac and Cry2Ab in 96% of transgenic cotton samples, highlighting effective ELISA and PCR techniques.
To develop BGII hybrids/varieties, the elite lines which were proven for high yield with jassid resistance were selected and converted under BGII background for further usage in BGII hybrid development programme. Hence, the study was aimed to detect the presence of Cry1Ac and Cry2Ab proteins/genes through qualitative ELISA, PCR techniques and to select the homozygous population from the segregating generations consisting of 1663 samples from different segregating generations as well as from stabilized populations from OYT/PYT/AYT yield trials. The study revealed that out of 9125 samples, 8760 (96%) of samples showed the presence of cry 1Ac and cry 2Ab proteins in the transgenic leaf samples and also demonstrated that the technique of ELISA for identification of cry 1Ac and cry 2Ab proteins is quite handy and easily adoptable. Using PCR technique, the zygosity status of the samples were known for cry1Ac and cry2Ab genes; used for selection and advancement to next generations in the breeding programme.
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Chapara et al. (2025) studied this question.
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