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Regeneration of plantlets from hypocotyl-derived callus of Coptis teeta

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Abstract

Callus cultures of Coptis teeta were established from hypocotyl segments (excised from aseptically germinating seeds) on Murashige and Skoog (MS) medium containing 2,4-dichlorophenoxyacetic acid (2,4-D) and kinetin. Microshoots were produced within 6–7 weeks of subculturing this callus in 1/2 MS nutrient medium supplemented with kinetin alone. Excised microshoots were rooted in 1/2 MS nutrient medium containing indolebutyric acid (IBA). The complete plantlets were hardened and established.

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Tandon, P., Rathore, T.S. Regeneration of plantlets from hypocotyl-derived callus of Coptis teeta . Plant Cell Tiss Organ Cult 28, 115–117 (1992). https://doi.org/10.1007/BF00039923

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  • DOI: https://doi.org/10.1007/BF00039923

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