Cryopreservation of embryogenic cell suspensions of Catharanthus roseus L. (G)Don.
Tipo de material:
TextoSeries ; Plant Cell, Tissue and Organ Culture , 98, p.1-9, 2009Trabajos contenidos: - Fatima, S
- Mujib, A
- Nasim, S.A
- Siddiqui, Z.H
| Item type | Current library | Collection | Call number | Status | Date due | Barcode | |
|---|---|---|---|---|---|---|---|
Documentos solicitados
|
CICY Documento préstamo interbibliotecario | Ref1 | B-10853 (Browse shelf(Opens below)) | Available |
An efficient cryopreservation protocol was established for embryogenic cell suspension cultures of Catharanthus roseus. This involved a vitrification-based cryopreservation method wherein embryogenic cells were exposed to a preculture/pretreatment medium prior to their immersion in liquid nitrogen. These cell suspension cultures were first initiated from friable embryogenic callus derived from hypocotyls of C. roseus on a medium containing 4.52 lM 2,4-Dichlorophenoxy acetic acid (2, 4-D). Among different sucrose (0.09-0.6 M)and sorbitol (0.2-0.6 M)levels evaluated during preculture, 0.4 M sucrose promoted highest cellular regrowth. Whereas, among pretreatments Dimethyl sulphoxide (DMSO)(5 or 10
There are no comments on this title.
