Purpose: Due to pharmaceutical value of Stevia plant (Stevia rebudiana Bertoni.), this study was done to introduce a new protocol for rapid mass propagation of itthrough tissue culture. Research Method: In MS medium shoot proliferation of stevia by six concentrations of BA (0, 0.1, 0.2, 0.3, 0.4, 0.5 mg·l-1) and root induction by four concentrations of IBA (0, 0.025, 0.05, 0.1 mg·l-1) was investigated.Rooting of cuttings was done both in vitro and ex vivo conditions. Findings: According to the results, the most number of stems obtained in MS medium containing 0.3 mg l-1 BA. The highest length of stems obtained in MS medium without BA and the most number of leaves observed in MS medium supplemented with 0.4 mg·l-1 BA. In in vitro situation, ...
In the preceding research, stevia has been typically cloned in vitro using two media, on which the s...
Stevia rebaudiana Bertoni is a medicinal plants and commercially use as non-caloric sweetener for di...
ABSTRACT In order to develop a protocol for high efficiency in vitro regeneration of two cultivars o...
Stevia rebaudiana Bertoni has sweet substances (stevioside) in its leaves that are free of calories ...
Stevia rebaudiana Bertoni has sweet substances (stevioside) in its leaves that are free of calories ...
Background: Stevia rebaudiana Bertoni is one of the most amazing herb that is an abundant source of ...
Background: Stevia rebaudiana Bertoni, an important anti-diabetic medicinal plant, becomes an inevit...
Liquid shoot culture of Stevia rebaudiana Bertoni in MS medium containing BAP (1.5 mg/l) and IAA (0....
Callusing response of various field grown and in vitro grown explants such as leaf was studied using...
A plant tissue culture protocol from stevia was optimized for the production of planting materials a...
Stevia rebaudiana commonly known as “Stevia” is a native herb of South America. The leaves of stevi...
Plant regeneration through indirect organogenesis allows obtaining genetic variability that can be u...
Propagation of S. rebaudiana Bertoni can be done by seed germination and stem cutting. Seed germinat...
A plant tissue culture protocol from stevia was optimized for the production of planting materials a...
Stevia rebaudiana Bertoni is a important medicinal plant which is mostly know as a sugar substitute....
In the preceding research, stevia has been typically cloned in vitro using two media, on which the s...
Stevia rebaudiana Bertoni is a medicinal plants and commercially use as non-caloric sweetener for di...
ABSTRACT In order to develop a protocol for high efficiency in vitro regeneration of two cultivars o...
Stevia rebaudiana Bertoni has sweet substances (stevioside) in its leaves that are free of calories ...
Stevia rebaudiana Bertoni has sweet substances (stevioside) in its leaves that are free of calories ...
Background: Stevia rebaudiana Bertoni is one of the most amazing herb that is an abundant source of ...
Background: Stevia rebaudiana Bertoni, an important anti-diabetic medicinal plant, becomes an inevit...
Liquid shoot culture of Stevia rebaudiana Bertoni in MS medium containing BAP (1.5 mg/l) and IAA (0....
Callusing response of various field grown and in vitro grown explants such as leaf was studied using...
A plant tissue culture protocol from stevia was optimized for the production of planting materials a...
Stevia rebaudiana commonly known as “Stevia” is a native herb of South America. The leaves of stevi...
Plant regeneration through indirect organogenesis allows obtaining genetic variability that can be u...
Propagation of S. rebaudiana Bertoni can be done by seed germination and stem cutting. Seed germinat...
A plant tissue culture protocol from stevia was optimized for the production of planting materials a...
Stevia rebaudiana Bertoni is a important medicinal plant which is mostly know as a sugar substitute....
In the preceding research, stevia has been typically cloned in vitro using two media, on which the s...
Stevia rebaudiana Bertoni is a medicinal plants and commercially use as non-caloric sweetener for di...
ABSTRACT In order to develop a protocol for high efficiency in vitro regeneration of two cultivars o...