Plant Culture Media

Basal salt mixture containing micro and macro elements as described by Murashige and Skoog (1962). MES buffer 500 mg/L added to prevent acidification during cultivation. Supplied as powder. Concentration: 4802.1 mg/L Hygroscopic

Basal salt mixture containing micro and macro elements as described by Murashige and Skoog (1962). MES buffer 500 mg/L added to prevent acidification during cultivation. Supplied as powder. Concentration: 4802.1 mg/L Hygroscopic

Basal salt mixture containing micro and macro elements as described by Murashige and Skoog (1962). MES buffer 500 mg/L added to prevent acidification during cultivation. Supplied as powder. Concentration: 4802.1 mg/L Hygroscopic

Basal salt mixture containing micro and macro elements as described Murashige and Skoog (1962) and vitamins as described by Nitsch & Nitsch (1969). Supplied as powder. Concentration: 4410.64 mg/L Hygroscopic

Basal salt mixture containing micro and macro elements as described by Murashige & Skoog (1962). Modified by replacing FeNaEDTA with FeEDDHA as described by Van der Salm et. al. (1994). Concentration: 4464.49 mg/L Hygroscopic

Basal salt mixture containing micro and macro elements as described by Murashige & Skoog (1962). Modified by replacing FeNaEDTA with FeEDDHA as described by Van der Salm et. al. (1994). Concentration: 4464.49 mg/L Hygroscopic

Basal salt mixture containing micro and macro elements as described by Murashige & Skoog (1962). Modified by replacing FeNaEDTA with FeEDDHA as described by Van der Salm et. al. (1994). Concentration: 4464.49 mg/L Hygroscopic

Murashige and Skoog Medium (MS) was originally formulated by Murashige and Skoog in 1962 to optimize tobacco callus bioassay system for facilitating the study of cytokinins. Since then, it is widely used for micro propagation, organ culture, callus

Murashige and Skoog Medium (MS) was originally formulated by Murashige and Skoog in 1962 to optimize tobacco callus bioassay system for facilitating the study of cytokinins. Since then, it is widely used for micro propagation, organ culture, callus

Murashige and Skoog Medium (MS) was originally formulated by Murashige and Skoog in 1962 to optimize tobacco callus bioassay system for facilitating the study of cytokinins. Since then, it is widely used for micro propagation, organ culture, callus

Murashige and Skoog Medium (MS) was originally formulated by Murashige and Skoog in 1962 to optimize tobacco callus bioassay system for facilitating the study of cytokinins. Since then, it is widely used for micro propagation, organ culture, callus

Murashige and Skoog Medium (MS) was originally formulated by Murashige and Skoog in 1962 to optimize tobacco callus bioassay system for facilitating the study of cytokinins. Since then, it is widely used for micro propagation, organ culture, callus