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Date Palm Biotechnology Protocols Volume II

Overview of attention for book
Date Palm Biotechnology Protocols Volume II
Springer New York

Table of Contents

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    Book Overview
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    Chapter 1 Storage and Viability Assessment of Date Palm Pollen
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    Chapter 2 In Vitro Conservation of Date Palm Tissue Cultures
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    Chapter 3 Cryopreservation of Date Palm Pro-Embryonic Masses Using the D Cryo-plate Technique
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    Chapter 4 In Vitro Cryopreservation of Date Palm Caulogenic Meristems
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    Chapter 5 In Vitro Conservation of Date Palm Shoot-Tip Explants and Callus Cultures Under Minimal Growth Conditions
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    Chapter 6 In Vitro Conservation of Date Palm Somatic Embryos Using Growth-Retardant Conditions
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    Chapter 7 Encapsulation of Date Palm Somatic Embryos: Synthetic Seeds
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    Chapter 8 Evaluation of Clonal Fidelity of Micropropagated Date Palm by Random Amplified Polymorphic DNA (RAPD)
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    Chapter 9 Molecular Identification of Fungal Contamination in Date Palm Tissue Cultures
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    Chapter 10 Genetic Diversity Analysis of Date Palm Using Random Amplified Polymorphic DNA (RAPD) and Inter-Simple Sequence Repeat (ISSR)
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    Chapter 11 Date Palm Genetic Diversity Analysis Using Microsatellite Polymorphism
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    Chapter 12 Assessing Date Palm Genetic Diversity Using Different Molecular Markers
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    Chapter 13 Molecular Analysis of Date Palm Genetic Diversity Using Random Amplified Polymorphic DNA (RAPD) and Inter-Simple Sequence Repeats (ISSRs)
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    Chapter 14 Determining Phylogenetic Relationships Among Date Palm Cultivars Using Random Amplified Polymorphic DNA (RAPD) and Inter-Simple Sequence Repeat (ISSR) Markers
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    Chapter 15 Genotyping and Molecular Identification of Date Palm Cultivars Using Inter-Simple Sequence Repeat (ISSR) Markers
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    Chapter 16 Molecular Identification of Date Palm Cultivars Using Random Amplified Polymorphic DNA (RAPD) Markers
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    Chapter 17 Early Sex Identification in Date Palm by Male-Specific Sequence-Characterized Amplified Region (SCAR) Markers
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    Chapter 18 Gender Identification in Date Palm Using Molecular Markers
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    Chapter 19 Development of Sex-Specific PCR-Based Markers in Date Palm
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    Chapter 20 Date Palm Sex Differentiation Based on Fluorescence In Situ Hybridization (FISH)
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    Chapter 21 Characterization and Amplification of Gene-Based Simple Sequence Repeat (SSR) Markers in Date Palm
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    Chapter 22 Mitochondrial Molecular Markers for Resistance to Bayoud Disease in Date Palm
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    Chapter 23 Analysis of Expressed Sequence Tags (EST) in Date Palm
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    Chapter 24 Development of Genomic Simple Sequence Repeats (SSR) by Enrichment Libraries in Date Palm
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    Chapter 25 MicroRNA Expression in Multistage Date Fruit Development
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    Chapter 26 Proteome of Abiotic Stress Tolerance in Date Palm
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    Chapter 27 Electrophoresis-Based Proteomics to Study Development and Germination of Date Palm Zygotic Embryos
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    Chapter 28 Date Fruit Proteomics During Development and Ripening Stages
Attention for Chapter 7: Encapsulation of Date Palm Somatic Embryos: Synthetic Seeds
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Chapter title
Encapsulation of Date Palm Somatic Embryos: Synthetic Seeds
Chapter number 7
Book title
Date Palm Biotechnology Protocols Volume II
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7159-6_7
Pubmed ID
Book ISBNs
978-1-4939-7158-9, 978-1-4939-7159-6
Authors

Shawky A. Bekheet

Abstract

Synthetic seed or encapsulated somatic embryos may be used for propagation, storage, and exchange of plant germplasm and have many diverse applications in date palm cultivation. They have advantages over conventional use of offshoot material for germplasm propagation, maintenance, exchange, and transportation. This chapter describes a protocol for date palm synthetic seed production by encapsulation of somatic embryos with sodium alginate. Among three concentrations used, 3% sodium alginate followed by dropping into 2.5% calcium chloride (CaCl2) solution shows the best concentration of gel matrix for both maintenance and recovery. In addition, storage of the encapsulated date palm somatic embryos at 5 °C improves the survival and conversion into plantlets; otherwise, 20 g/L sucrose in the culture medium enhances conversion of the recovered somatic embryos to plantlets. This protocol is promising for in vitro conservation and international exchange of date palm germplasm.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 13%
Professor 1 13%
Student > Doctoral Student 1 13%
Unknown 5 63%
Readers by discipline Count As %
Unspecified 1 13%
Biochemistry, Genetics and Molecular Biology 1 13%
Unknown 6 75%