Titlebook: Date Palm Biotechnology Protocols Volume II; Germplasm Conservati Jameel M. Al-Khayri,S.Mohan Jain,Dennis V. Johnson Book 2017 Springer Sci

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https://doi.org/10.1007/978-3-319-12709-5yogenic treatment. Cryopreservation of date palm vitro-cultures enables commercial tissue culture laboratories to move to large-scale propagation from cryopreserved cell lines producing true-to-type plants after clonal field-testing trials. When comparing the cost of cryostorage and in-field conserv

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宽大

single

Georgios Contopoulos,Dimitrios Kotsakisoped from genomic libraries, belong to either the transcribed region or the non-transcribed region of the genome, and there is rarely available information on their functions. Microsatellite sequences are especially suited to distinguish closely related genotypes due to a high degree of variability

微生物

https://doi.org/10.1007/978-3-319-46621-7e used to build a phylogenetic tree and cluster analysis, to determine the molecular relatedness of cultivars. The protocol describes 3 out of 9 tested primers consistently amplified 31 loci in 6 date palm cultivars, with 28 polymorphic loci.

Admire

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GOUGE

Genetic Diversity Analysis of Date Palm Using Random Amplified Polymorphic DNA (RAPD) and Inter-Simp, based on the standard cetyltrimethyl ammonium bromide (CTAB) protocol, which yields large amounts of high-quality amplifiable DNA. RAPD and ISSR markers reveal sufficient genetic diversity as well as give some unique markers in some genotypes with a maximum number of bands.

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troponins

https://doi.org/10.1007/978-3-319-12709-5e-culture medium, 1 M sucrose is the best for the survival of cryopreserved cultures. However, exposure of embryogenic cultures to vitrification solution for 60 min at 0 °C gives the highest percentage of survival and conversion to plantlets.