| dc.contributor.author | Bajwa, Amna Ali, Rukhsana | |
| dc.date.accessioned | 2013-03-20T09:40:25Z | |
| dc.date.accessioned | 2019-05-29T05:10:01Z | |
| dc.date.available | 2013-03-20T09:40:25Z | |
| dc.date.available | 2019-05-29T05:10:01Z | |
| dc.date.issued | 2013-01 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.11948/871 | |
| dc.description.abstract | The molecular study is based on genomic DNA therefore DNA must be extracted in a pure and uncontaminated form. In this study, genomic DNA of twenty four isolates of Trichoderma species (T. harzianum, T. hamatum, T. koningii and T. pseudokoningii) indicated band of ~15Kb on 0.8% agarose gel and quality was determined by obtaining absorbance ratio (260/280) in the range of 1.7-1.9. Restriction fragment length polymorphism (RFLP) analyses were performed by using two restriction endonulease enzymes i.e., BamHI and HindIII. The BamHI represented results in the range of 500bp-750bp. 18S rRNA gene targeting was further carried out through optimization in ribotyping analysis. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Daffodil International University | en_US |
| dc.subject | Trichoderma harzianum, T. hamatum, T. koningii, T. pseudokoningii RFLP, restriction endonuleases, 18S rRNA. | en_US |
| dc.title | MOLECULAR SCREENING OF TRICHODERMA ISOLATES | en_US |
| dc.type | Article | en_US |