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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/17470
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dc.contributor.authorRen Wang-
dc.contributor.authorLi-Si He-
dc.contributor.authorBing Xia-
dc.contributor.authorTong, Jin-Feng-
dc.contributor.authorNing Li-
dc.contributor.authorFeng Peng-
dc.date.accessioned2023-03-06T06:56:38Z-
dc.date.available2023-03-06T06:56:38Z-
dc.date.issued2009-04-20-
dc.identifier.citationWang, R., He, L. S., Xia, B., Tong, J. F., Li, N., & Peng, F. (2009). A micropropagation system for cloning of hemp (Cannabis sativa L.) by shoot tip culture. Pak. J. Bot, 41(2), 603-608.en_US
dc.identifier.issn0556-3321-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/17470-
dc.description.abstractThis study describes the standardization of an efficient in vitro propagation and hardening procedure for obtaining plantlets from shoot tips of Hemp (Cannabis sativa L.). Hemp seedlings were germinated on half-strength 1/2 MS medium supplemented with 10 g·L-1sucrose, 5.5 g·L-1agar at a pH of 6.8 under light for 16 h per day. MS medium containing 0.2 mg·L-1TDZ, 0.1 mg·L-1NAA supported the maximal auxiliary bud multiplication rate of 3.22 per shoot tip. The proliferated buds were successfully rooted on MS medium supplemented with 0.1 mg·L-1IBA and 0.05 mg·L-1NAA resulting in 85% of the plantlets rooting. The procedure requires a 54 days cycle for the In vitro clonal propagation (14 days for shoot multiplication and 40 days for root induction) which includes 35-42 days for acclimatized plantlet production.en_US
dc.language.isoenen_US
dc.publisherKarachi: Pakistan Botanical Society, University of Karachien_US
dc.titleA MICROPROPAGATION SYSTEM FOR CLONING OF HEMP (CANNABIS SATIVA L.) BY SHOOT TIP CULTUREen_US
dc.typeArticleen_US
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