Experiment was designed and conducted to determine the most appropriate concentration of 2, 4-Dichlorophenoxy Acetic Acid suitable for callus induction in sugarcane. Explants were obtained from apical meristems of two sugarcane cultivars (SP726180 and CO-001) and cultured in a modified MS medium supplemented with varying concentrations of 2,4-D. After sterilization, the explants were incubated in the growth chamber at 270C and monitored for callus induction for four Weeks. The resulting calli were sub cultured on a media with a reduced 2,4-D concentration to induce somatic embryogenesis. Percentages of callus formation, embryogenic callus as well as growth coefficient were the parameters monitored. Data generated were analyzed using Chi-squ...
Not AvailableStudies were carried out to establish an efficient system for in vitro regeneration of ...
Induction of in vitro sugarcane through somatic embryogenesis technique influenced by addition of pl...
We have developed a new, simple, quick and genotype-independent method for direct regeneration of ...
Sugarcane is an important perennial, polyploidy crop. Based on the growing demand, it has now attrac...
The aim of this study was to establish a protocol for induction of somatic embryogenesis and regener...
Sugarcane (Saccharum officinarum L.) is an economically important crop in S...
The effect of genotype and 2, 4-D on callogenesis was investigated in sugarcane (Saccharum spp.) hyb...
In vitro regeneration of sugarcane (Saccharum officinarum L.) clones can support breeding program of...
Twelve commercial sugarcane (Saccharum spp. hybrids) varieties were compared for both their ability ...
Nine sugarcane genotypes (CP59-73, CP63-588, CP80-314, SP71-1081, F160, L62-96, CP70-321, CP57- 614 ...
In vitro regeneration of sugarcane (Saccharum officinarum L.) clones can support breeding program of...
The development of an efficient regeneration system is crucial for the genetic transformation of sug...
Sugarcane (Saccharum officinarum L) var. 668 was propagated through tissue culture technique: callog...
332-334Callus cultures were established in three commercial sugarcane varieties, viz., CoJ 64, CoJ 8...
Two commercial cultivars (CPF-245 and CPF-237) and three advanced lines (CSSG-668, S-2003US633, S-20...
Not AvailableStudies were carried out to establish an efficient system for in vitro regeneration of ...
Induction of in vitro sugarcane through somatic embryogenesis technique influenced by addition of pl...
We have developed a new, simple, quick and genotype-independent method for direct regeneration of ...
Sugarcane is an important perennial, polyploidy crop. Based on the growing demand, it has now attrac...
The aim of this study was to establish a protocol for induction of somatic embryogenesis and regener...
Sugarcane (Saccharum officinarum L.) is an economically important crop in S...
The effect of genotype and 2, 4-D on callogenesis was investigated in sugarcane (Saccharum spp.) hyb...
In vitro regeneration of sugarcane (Saccharum officinarum L.) clones can support breeding program of...
Twelve commercial sugarcane (Saccharum spp. hybrids) varieties were compared for both their ability ...
Nine sugarcane genotypes (CP59-73, CP63-588, CP80-314, SP71-1081, F160, L62-96, CP70-321, CP57- 614 ...
In vitro regeneration of sugarcane (Saccharum officinarum L.) clones can support breeding program of...
The development of an efficient regeneration system is crucial for the genetic transformation of sug...
Sugarcane (Saccharum officinarum L) var. 668 was propagated through tissue culture technique: callog...
332-334Callus cultures were established in three commercial sugarcane varieties, viz., CoJ 64, CoJ 8...
Two commercial cultivars (CPF-245 and CPF-237) and three advanced lines (CSSG-668, S-2003US633, S-20...
Not AvailableStudies were carried out to establish an efficient system for in vitro regeneration of ...
Induction of in vitro sugarcane through somatic embryogenesis technique influenced by addition of pl...
We have developed a new, simple, quick and genotype-independent method for direct regeneration of ...