000 | 01896cam a2200325 a 4500 | ||
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003 | EG-GiCUC | ||
008 | 190416s2018 ua d f m 000 0 eng d | ||
040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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041 | 0 | _aeng | |
049 | _aDeposite | ||
097 | _aPh.D | ||
099 | _aCai01.07.12.Ph.D.2018.As.I | ||
100 | 0 | _aAsmaa Elsayed Abdelhafez | |
245 | 1 | 0 |
_aIn vitro study on the propagation , conservation and DNA of Odontonema cuspidatum (Nees) O.Ktze Plant / _cAsmaa Elsayed Abdelhafez ; Supervised Salwa Salem Sakr , Mohamed Abdelkhalek Elkhateeb , Mamdouh Ahmed Elshamy |
246 | 1 | 5 | _aOdontonema cuspidatum دراسة معملية على الاكثار و الحفظ و الحمض النووى لنبات |
260 |
_aCairo : _bAsmaa Elsayed Abdelhafez , _c2018 |
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300 |
_a155 P. : _bcharts ; _c25cm |
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502 | _aThesis (Ph.D.) - Cairo University - Faculty of Agriculture - Department of Ornamental Horticulture | ||
520 | _aThis investigation was carried out during the period from 2014 to 2017. Using NaOCl at 2% for 25 min was the most effective. Culturing of the explants on full MS medium supplemented with 0.5 mg/l TDZ, was positively, 1mg/l IBA and 2 mg/l NAA resulted in the highest number of roots. peat moss+ sand at the ratio of 3:1 (v/v) to acclimatization. For encapsulation used sodium alginate (5 %) and 1.1 g/100ml CaCl2.2H2o2. Using sucrose at 50 g/l as osmotic agent was the best in all storage periods. RAPD- based DNA fingerprints gave no eridence of on variation during in vitro conservation | ||
530 | _aIssued also as CD | ||
653 | 4 | _aIn vitro | |
653 | 4 | _aMicropropagation | |
653 | 4 | _aTissue culture | |
700 | 0 |
_aMamdouh Ahmed Elshamy , _eSupervisor |
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700 | 0 |
_aMohamed Abdelkhalek Elkhateeb , _eSupervisor |
|
700 | 0 |
_aSalwa Salem Sakr , _eSupervisor |
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905 |
_aAsmaa _eCataloger |
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905 |
_aNazla _eRevisor |
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942 |
_2ddc _cTH |
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999 |
_c71490 _d71490 |